Incorporation of internal polya-encoded poly-lysine sequence tags and their variations for the tunable control of protein synthesis in bacterial and eukaryotic cells

ABSTRACT

The present disclosure relates to modulation of protein expression.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 16/317,791, filed Jan. 14, 2019 which claims the benefit of PCT Application number PCT/US17/41766, filed Jul. 12, 2017, which claims the benefit of U.S. Provisional Application 62/361,307, filed Jul. 12, 2016, U.S. Provisional Application No. 62/427,518, filed Nov. 29, 2016, U.S. Provisional Application No. 62/437,464, filed Dec. 21, 2016, and U.S. Provisional Application No. 62/438,017, filed Dec. 22, 2016, each of the disclosures of which is hereby incorporated by reference in its entirety.

GOVERNMENTAL RIGHTS

This invention was made with government support under T32 GM007067 and RO1 GM112824 awarded by the National Institutes of Health (NIH). The government has certain rights in the invention.

REFERENCE TO A SEQUENCE LISTING

This application contains a Sequence Listing that has been submitted in Extensible Markup Language (.xml) and is hereby incorporated by reference in its entirety. The XML copy, created on Mar. 13, 2023, is named 047563-755867.xml, and is 148.025 bytes in size.

FIELD OF THE INVENTION

The present disclosure relates to modulation of protein expression.

BACKGROUND OF THE INVENTION

Gene expression in cells is a multistep process that involves transcription of genetic material from DNA to RNA and ultimately translation of mRNA into protein. These processes are subject to stringent control at all levels. Translational regulation generally controls the amount of protein generated from a given mRNA. While a majority of translational regulation mechanisms target the recruitment of ribosomes to the initiation codon, the protein synthesis machinery can also modulate translation, elongation, and termination (Dinman and Berry (2007) Cold Spring Harb. Monogr.Arch.; Hershey et al. (2012) Cold Spring Harb. Perspect. Biol. 4).

Pausing during the translational cycle—so-called ribosome stalling—is one mechanism by which the level of translation elongation can be regulated. Ribosome stalling is recognized by components of mRNA surveillance pathways, no-go decay (NGD) and non-stop decay (NSD), resulting in endonucleolytic cleavage of the stalled mRNA, ribosome rescue and proteolytic degradation of incomplete protein products (Shoemaker and Green (2012) Nat. Struct. Mol. Biol. 19, 594-601). NGD and NSD act on aberrant mRNAs that trigger translational arrest, as observed with damaged bases, stable stem-loop structures (Doma and Parker (2006) Nature 440, 561-564), rare codons (Letzring et al. (2010) RNA N. Y. N. 16, 2516-2528) or mRNAs lacking stop codons (non-stop mRNAs) (Dimitrova et al. (2009) J. Biol. Chem. 284, 10343-10352). However, these mechanisms also act on more specific types of translational pauses, such as runs of codons that encode consecutive basic amino acids (Kuroha et al. (2010) EMBO Rep. 11, 956-961; Brandman et al. (2012) Cell 151,1042-1054). It is thought that polybasic runs, as well as translation of the poly(A) tail in the case of non-stop mRNAs, cause ribosome stalling through interaction of the positively charged peptide with the negatively charged ribosome exit channel (Lu and Deutsch (2008) J. Mol. Biol. 384, 73-86). Presumably, the strength of the stall is dependent on the length and composition of the polybasic stretch, and thus the impact on overall protein expression might vary (Shoemaker and Green (2012) Nat. Struct. Mol. Biol. 19, 594-601). Given this logic, it seems plausible that such an amino acid motif may act as a gene regulatory element that would define the amount of protein translated and the stability of the mRNA. For example, structural and biophysical differences between lysine and arginine residues as well as potential mRNA sequence involvement could act to further modulate this process.

Most studies investigating the effects of polybasic sequences during translation have used reporter sequences in E. coli (Koutmou et al. (2015) eLIFE 10.7554/eLife.05534), yeast (Brandman et al. (2012) Cell 151, 1042-1054; Tsuboi et al. (2012) Mol. Cell. 46, 518-529) or in vitro rabbit reticulocyte lysate (Lu and Deutsch (2008) J. Mol. Biol. 384, 73-86). However, detailed mechanistic information about the nature of the stall in endogenous targets through genome-wide analyses has not yet been conducted.

SUMMARY OF THE INVENTION

In an aspect, the disclosure provides a method for modulating the level of expression of a polypeptide in a cell, the method comprising modulating the amount of consecutive adenine (A) nucleotides in at least one lysine codon in an open reading frame of a polynucleotide sequence encoding the polypeptide in the cell, thereby modulating the level of expression of the polypeptide in the cell.

In another aspect, the disclosure provides an expression vector comprising: a) a cloning site for inserting at least one polynucleotide sequence encoding a polypeptide to be expressed, and at least one polynucleotide tag sequence comprising at least one AAG lysine codon that increases expression of the at least one polynucleotide sequence when the expression vector is introduced into a cell; or b) a cloning site for inserting at least one polynucleotide sequence encoding a polypeptide to be expressed, and at least one polynucleotide tag sequence comprising at least one AAA lysine codon that decreases expression of the at least one polynucleotide sequence when the expression vector is introduced into a cell.

In another aspect, the disclsoure provides an expression vector comprising: a) at least one engineered polynucleotide sequence encoding a polypeptide to be expressed, the at least one engineered polynucleotide sequence comprising at least one engineered synonymous mutation of at least one AAA lysine codon to at least one AAG lysine codon in a coding sequence of the at least one polynucleotide sequence, wherein the synonymous mutation increases expression of the polypeptide to be expressed when the expression vector is introduced into a cell; or b) at least one engineered polynucleotide sequence encoding a polypeptide to be expressed, the at least one engineered polynucleotide sequence comprising at least one engineered synonymous mutation of at least one AAG lysine codon to at least one AAA lysine codon in a coding sequence of the at least one polynucleotide sequence, wherein the synonymous mutation decreases expression of the polypeptide to be expressed when the expression vector is introduced into a cell.

In yet another aspect, the disclosure provides a method of decreasing translation of a protein in a cell, by increasing the quantity of consecutive adenine nucleotides in an open reading frame (ORF) or an untranslated region (UTR) adjacent to the ORF in genomic DNA (gDNA). The gDNA may be modified by using a clustered regularly interspaced short palindromic repeats (CRISPR) enzyme system, zinc-finger nuclease (ZFN), or transcription activator-like effector nuclease (TALEN).

BRIEF DESCRIPTION OF THE FIGURES

The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

FIG. 1A and FIG. 1B show the distribution of polyarginine (FIG. 1A) and polylysine (FIG. 1B) runs of different length in several organisms. Abundance is normalized to the number of residues of certain kind in all protein isoforms (see Materials and Methods, Example 1).

FIG. 2A, FIG. 2B, FIG. 2C, and FIG. 2D show a cartoon of reporter constructs used in electroporation experiments (FIG. 2A), western blot analyses of HA-X-mCherry constructs 48 hours after electroporation (FIG. 2B; HA and β-actin antibodies), normalized protein expression using Licor western blot analyses or in vivo mCherry fluorescence measurement (FIG. 2C; β-actin or fluorescence of co-expressed GFP construct were used for normalization of the data, respectively; each bar represents percentage of wild type mCherry (WT) expression/fluorescence), and normalized RNA levels of HA-X-mCherry constructs (FIG. 2D; neomycin-resistance gene was used for normalization of qRT-PCR data; each bar represents percentage of wild type mCherry (WT) mRNA levels).

FIG. 3A and FIG. 3B show the expression of HA-X-mCherry reporters in Chinese Hamster Ovary cells. Western blot analysis of reporter expression was normalized to β-actin levels (FIG. 3A). qRT-PCR analyses of mRNA abundance was normalized to neomycin resistance gene and presented as fraction of mRNA levels for mCherry construct without insert (FIG. 3B).

FIG. 4A and FIG. 4B show the expression of HA-X-mCherry reporters in Drosophila S2 cells. Western blot analysis of reporter expression was normalized to total protein amount (FIG. 4A). qRT-PCR analyses of mRNA abundance was normalized to levels of endogenous GAPDH mRNA and presented as fraction of mRNA levels for mCherry construct without insert (FIG. 4B).

FIG. 5A and FIG. 5B show the expression of HA-X-mCherry reporters from T7-RNA polymerase in vitro transcribed mCherry mRNAs in neonatal human fibroblasts (HDFs). HA-MBP mRNAs were in vitro transcribed and co-electroporated into HDFs as a control for electroporation efficiency and western blot normalization. β-actin was used as a control for the total protein amounts (FIG. 5A). Each lane was subjected to Bio-Rad quantification analyses to determine the levels of expression shown on the graph below (FIG. 5B).

FIG. 6A, FIG. 6B, and FIG. 6C show the differential stability of electroporated mRNAs from HA-X-mCherry reporters is translation dependent. In vitro transcribed mCherry mRNAs were electroporated in HDFs. Protein (FIG. 6A) and mRNA (FIG. 6B) levels were assessed by western blot analyses or qRT-PCR. HA-(AAA)12-mCherry construct shows significant reduction in protein levels as well as in mRNA stability. Addition of translation initiation inhibitor, herringtonine, completely abolishes effect on mRNA stability (FIG. 6C).

FIG. 7A, FIG. 7B, and FIG. 7C show that insertion of polylysine mCherry constructs in the coding sequence results in the same protein reduction and decreased mRNA stability. FIG. 7A shows the scheme of assayed mCherry constructs. Thioredoxin (Trx) fusion protein was used instead of insertion of polylysine run in the middle of mCherry gene. Positions of 12 lysine (36As) insertions and HA-tagg in the constructs are labeled with blue and gray boxes, respectively. Numbers above reporter indicate distance of 36As insertion from the first nucleotide in the coding sequence. FIG. 7B shows that protein expression was monitored by western blot analyses using HA and beta-actin antibody. FIG. 7C shows that qRT-PCR analyses of mRNA abundance was normalized to neomycin resistance gene and presented as fraction of mRNA levels for WT mCherry construct without insert.

FIG. 8A, FIG. 8B, and FIG. 8C show the expression of HA-tagged hemoglobin (delta chain; HBD) constructs with natural introns in HDF cells. FIG. 8A shows a scheme of HBD gene with position of poly lysine and stop codon insertions. Position and length of introns as well as exons in HBD constructs are indicated. FIG. 8B shows western blot analysis of HA-HBD construct expression normalized to β-actin levels. FIG. 8C shows qRT-PCR analyses of mRNA abundance normalized to neomycin resistance gene and presented as fraction of mRNA levels for WT HBD construct without insert.

FIG. 9 shows a comparison of usage of AAA in single, double and triple lysine runs across several organisms. Expected values (black bars) are based on Kazusa database, while observed (yellow bars) are calculated from all isoforms of proteins available in NCBI RefSeq database.

FIG. 10 shows observed codon usage in all isoforms of human proteins vs. expected (based on the proportions 0.44 to 0.56, AAA to AAG for all lysines) in the tracks of four consecutive lysines. From top to bottom along the y-axis, the sequences correspond to SEQ ID NOs 71-86 respectively.

FIG. 11 shows codon distribution in four-lysine tracks in different organisms. All protein isoforms sequences and sequences of corresponding mRNAs were taken into account. The script checks all tracks of four consecutive lysines, even when overlapping (if there is a track of five lysines, it will report two nucleotide strings of length 12). From left to right along the x-axis, the sequences correspond to SEQ ID Nos 87-102 respectively.

FIG. 12A, FIG. 12B, FIG. 12C, FIG. 12D, and FIG. 12E shows HA-(A9-A13)-mCherry construct sequences and protein expression. FIG. 12A shows the cccupancy of ribosomal footprints for regions around different codon combinations for four lysine tracks. All combinations of one, two, three and four AAG codons per group are shown. Data for four AAA codons is not shown because only a single gene has such a sequence. The upper and lower “hinges” correspond to the first and third quartiles (the 25th and 75th percentiles). The upper and lower whiskers extend from hinges up or down at maximum of 1.5*IQR of the respective hinge. FIG. 12B shows the sequences of HA-(A9-A13)-mCherry constructs used in electroporation experiments. The WT nucleotide and amino acid sequences shown are SEQ ID NO: 71 and 72, respectively. The A9 nucleotide and amino acid sequences shown are SEQ ID NO: 10 and 73, respectively. The A10 nucleotide and amino acid sequences shown are SEQ ID NO: 11 and 73, respectively. The A11 nucleotide and amino acid sequences shown are SEQ ID NO: 12 and 74, respectively. The A12 nucleotide and amino acid sequences shown are SEQ ID NO: 13 and 75, respectively. The A14 nucleotide and amino acid sequences shown are SEQ ID 15 and 76, respectively. FIG. 12C shows western blot analyses of HA-(A9-A13)-mCherry constructs 48 hours after electroporation (HA and β-actin antibodies). FIG. 12D shows normalized protein expression using Licor western blot analyses or in vivo mCherry fluorescence measurement. β-actin or fluorescence of co-expressed GFP construct were used for normalization of the data, respectively. Each bar represents percentage of wild type mCherry (WT) expression/fluorescence. FIG. 12E shows normalized RNA levels of HA-X-mCherry constructs. Neomycin resistance gene was used for normalization of qRT-PCR data. Each bar represents percentage of wild type mCherry (WT) mRNA levels.

FIG. 13A and FIG. 13B show the occupancy of ribosomal footprints from three different data sets: FIG. 13A shows the region around polyA tracks and FIG. 13B shows the region around four arginine tracks, all codons combinations together. The upper and lower “hinges” correspond to the first and third quartiles (the 25th and 75th percentiles). The upper and lower whiskers extend from hinges at 1.5*IQR of the respective hinge.

FIG. 14A, FIG. 14B, FIG. 14C, and FIG. 14D show the sequences of polylysine runs from human genes incorporated into HA-X-mCherry constructs (FIG. 14A; continuous runs of lysine residues are labeled; number of lysine residues and ratio of AAG and AAA codons for each constructs are indicated), normalized protein expression using in vivo mCherry reporter fluorescence (FIG. 14B; fluorescence of co-transfected GFP was used to normalize the data; each bar represents percentage of wild type mCherry (WT) expression/fluorescence), normalized RNA levels of HA-X-mCherry constructs (FIG. 14C; neomycin resistance gene was used for normalization of qRT-PCR data; each bar represents percentage of wild type mCherry (WT) mRNA levels), and smoothed Gaussian kernel density estimate of positions of polyA tracks along the gene (FIG. 14D; position of polyA segment is expressed as a ratio between number of first residue of polyA track and length of a gene). In FIG. 14A, SLU7 is SEQ ID NO: 15; MTDH is SEQ ID NO: 16; NOP58 is SEQ ID NO: 17; ZCRB1 is SEQ ID NO: 18; and RASAL2 is SEQ ID NO: 19.

FIG. 15 shows the sequence conservation of RAS Activating-Like protein 2 gene (RASAL2) at DNA and protein sequence. Polylysine sequence and nucleotides forming polyA track are in indicated in red and bold letters, respectively. The amino acid sequence shown is SEQ ID NO: 111. The human, mouse, and hamster sequence shown is SEQ ID NO: 112. The pig sequence shown is SEQ ID NO: 113. The chicken sequence shown is SEQ ID NO: 114. The zebrafish sequence shown is SEQ ID NO: 114. The frog sequence shown is SEQ ID NO: 116.

FIG. 16A, FIG. 16B, FIG. 16C, FIG. 16D, FIG. 16E, and FIG. 16F show the scheme of constructs with ZCRB1 gene polyA tracks used for analyses of synonymous mutations (FIG. 16A), western blot analyses and normalized protein expression of ZCRB1 reporter constructs with synonymous mutations (FIG. 16B; HA and β-actin antibodies; each bar represents percentage of wild type ZCRB1-mCherry (WT) expression), normalized RNA levels of ZCRB1 reporter constructs with synonymous mutations (FIG. 16C; neomycin resistance gene was used for normalization of qRT-PCR data; each bar represents percentage of wild type ZCRB1-mCherry construct (WT) mRNA levels), the scheme of full-length HA-tagged ZCRB gene constructs (FIG. 16D; position and mutations in polyA tracks are indicated), western blot analysis and normalized protein expression of ZCRB1 gene constructs with synonymous mutations (FIG. 16E; each bar represents percentage of wild type HA-ZCRB1 (WT) expression, and normalized RNA levels of ZCRB1 gene constructs (FIG. 16F; neomycin resistance gene was used for normalization of qRT-PCR data). In FIG. 16A, the nucleotide sequence shown for ZCRB1 WT corresponds to nucleotides 3-30 of SEQ ID NO: 20; the nucleotide sequence shown for ZCRB1 411G>A corresponds to nucleotides 3-30 of SEQ ID NO: 21; the nucleotide sequence shown for ZCRB1 408A>G;417A>G corresponds to nucleotides 3-30 of SEQ ID NO: 22; and the amino acid sequence corresponds to residues 2-11 of SEQ ID NO: 77. In FIG. 16D, ZCRB1 WT is SEQ ID NO: 20; ZCRB1 411G>A is SEQ ID NO: 21; ZCRB1 408A>G;417A>G is SEQ ID NO: 22; and the amino acid sequence is SEQ ID NO: 77.

FIG. 17A, FIG. 17B, and FIG. 17C show synonymous mutations in mCherry reporter with metadherin (MTDH, Lyric(Lyr)) polyA track. FIG. 17A shows a scheme of reporter sequences with G>A and A>G synonymous mutations. The amino acid sequence shown is SEQ ID NO: 82, and the nucleotide sequences shown are SEQ ID NO: 78-81, respectively. FIG. 17B shows western blot analyses of reporter constructs with synonymous mutations. FIG. 17C shows normalized mRNA levels for reporter sequences with wild type MTDH polyA-track (Lwt) and corresponding mutants. mRNA levels are represented as fractions of wild type mCherry levels.

FIG. 18A, FIG. 18B, and FIG. 18C show synonymous mutations in mCherry reporter with RASAL2 polyA track. FIG. 18A shows a scheme of reporter sequences with G>A and A>G synonymous mutations. The amino acid sequence is SEQ ID NO: 83. The RASAL2 WT nucleic acid sequence corresponds to nucleotide 3032 of SEQ ID NO: 23. The RASAL2 G>A nucleic acid sequence corresponds to nucleotides 3-32 of SEQ ID NO: 24. The RASAL2 A>G nucleic acid sequence corresponds to nucleotides 3-32 of SEQ ID NO: 25. The RASAL2 A>G (3) nucleic acid sequence corresponds to nucleotides 3-32 of SEQ ID NO: 26. FIG. 18B shows western blot analyses of reporter constructs with synonymous mutations. FIG. 18C shows normalized mRNA levels for reporter sequences with wild type RASAL2 polyA-track (Lwt) and corresponding mutants. mRNA levels are represented as fractions of wild type mCherry levels.

FIG. 19A, FIG. 19B, FIG. 19C, and FIG. 19D show expression analysis of N-terminally HA- and C-terminaly GFP-tagged ZCRB1 gene and its synonymous mutants in HDF cells using Evos-FL microscopy. Cell images were taken 24 hours post electroporation using same optical settings. Cell nuclei were made visible using Hoechst 33342 dye. Images of HDF cells expressing double-tagged ZCRB1 wild type (WT) protein (FIG. 19A) ZCRB1 K137K:411 G>A (FIG. 19B) and ZCRB1 K136K:408 A>G; K139K:417 A>G (FIG. 19C) mutants. Images for each channel (trans, DAPI and GFP) were taken separately and overlay image was composed using EVOS FL digital software. FIG. 19D shows western blot analyses of HA-ZCRB1-GFP proteins from HDF cells using HA-antibody. Western blot analyses were normalized using beta-actin levels as loading controls.

FIG. 20A, FIG. 20B, FIG. 20C, and FIG. 20D show a scheme using luciferase constructs and luciferase expression. FIG. 20A shows immunoprecipitation of HA-ZCRB gene constructs using anti-HA magnetic beads. ZCRB1 WT, synonymous (single 411 G>A or double 408 A>G; 417 A>G), non-sense (385 G>T, insertion of stop codon prior poly(A) track), deletion (423ΔA, equivalent to +1 frame-shift) or insertion (423 A>AA, equivalent to −1 frame-shift) mutant constructs are labelled respectively. FIG. 20B shows a scheme of luciferase constructs used to estimate frame-shifting potential for ZCRB1 WT and 411 G>A mutant polyA tracks. FIG. 20C shows luciferase levels (activity) from −1, “zero” and +1 frame constructs of wild type and G>A mutant ZCRB1 polyA track are compared. Bars represent normalized ratio of ZCRB1 G>A and ZCRB1 WT poly(A) tracks elucidates changes in the levels of luciferase expression in all three frames. FIG. 20D shows a model for function of poly(A) tracks in human genes. Poly(A)-tracks lead to three possible scenarios: Frameshifting consolidated with NMD which results in reduced output of wild type protein; Frameshifting with synthesis of both out of frame and wild type protein; and non-resolved stalling consolidated by endonucleolytic cleavage of mRNA and reduction in wild type protein levels, as in NGD pathway. Scheme for translation of mRNAs without poly(A) tracks is shown for comparison.

FIG. 21A and FIG. 21B show that the introduction of COSMIC database reported synonymous mutation K447K (1341 G>A) in full length recombinant MTDH gene. FIG. 21A shows the sequence of the wild type and K447K (G>A) mutant of MTDH gene. The amino acid seqeunce shown is SEQ ID NO: 82, and the nucleotide sequences shown are SEQ ID NO: 78 and 90, respectively. FIG. 21B shows western blot analyses of HA-tagged WT and K474K mutant MTDH proteins. Major additional protein product corresponds to frame-shifted MTDH protein products (−1 and +1 FS) created by insertion or delation of one nucleotide following the last nucleotide in polyA-track.

FIG. 22A and FIG. 22B show the frame-shifting efficiency of polyA tracks from ZCRB1 WT (FIG. 22A) and ZCRB G>A mutant (FIG. 22B) measured by luciferase activity. Values for −1 and +1 frame-shifts (FS) for WT and mutant polyA track are presented as fractions of luciferase activity coming from expression from zero frame construct of WT (FIG. 22A) or mutant G>A sequence (FIG. 22B).

FIG. 23 shows the proportion of mutation types in polyA segments vs all mutation types. Data has been generated from COSMIC database. There is a dramatic shift in the distribution of mutations in polyA segments from substitutions (all COSMIC data) to frameshifts (polyA segments).

FIG. 24 shows the normalized distribution of lengths for polyA regions identified as 12 As allowing for one mismatch up to length 19 in human transcripts.

FIG. 25A, FIG. 25B, and FIG. 25C show design and mechanism of polyA track tag regulated gene expression. FIG. 25A shows scheme of inserted polyA tracks in the reporter genes used in this study. Hemagglutinin (HA) tag (gray) and polyA tracks (red) were introduced in the coding region of the reporter genes next to the start AUG codon. Exon boundaries as well as termination codon (Stop) are indicated. FIG. 25B shows proposed correlation between gene products levels, mRNA and protein, and the length of inserted polyA track tags. The reduction in levels of both reporter protein and mRNA is dependent on increasing length of consecutive adenine nucleotides in the coding sequence. FIG. 25C shows scheme of translation of eukaryotic reporter mRNA with or without inserted polyA tracks. The length of inserted polyA track tag determines the protein output of the regulated reporter gene as indicated by the number of globular protein structures. Features of the eukaryotic mRNAs (m7GpppG—cap, AUG—start codon, Stop—termination codon and polyA tail), as well as HA-tag, position of the polyA track tag, ribosome and nascent polypeptide chain are illustrated in the scheme.

FIG. 26A, FIG. 26B, FIG. 26C, FIG. 26D, FIG. 26E, and FIG. 26F show regulation of reporter gene by polyA tracks in the single cell prokaryotic and eukaryotic organisms. FIG. 26A shows percentage of mCherry fluorescence of tested LysAAG ((AAG)6-12) and LysAAA((AAA)3-12) insertion constructs compared to wild type fluorescence (WT, no insertion construct) 2 hours after promoter induction with 0.1% arabinose (w/v) in the media. mCherry fluorescence was assayed at excitation wavelength of 475±9 nm and emission was detected at 620±9 nm. Error bars indicate mean mCherry fluorescence values±standard deviation for three individual E. coli colonies for each construct. Background levels of mCherry expression can be estimated from the fluorescence of the wild type construct that was not induced with the addition of arabinose in the media (WT(NI)). FIG. 26B shows set of constructs analyzed for mCherry fluorescence was additionally assessed for protein expression levels by Western blot analysis. Equal amounts of E. coli cell lysates with Thioredoxin(Trx) fusion proteins were used for analysis. Fusion proteins were detected using HA-tag specific antibody. Positions of the fusion protein (Trx-HA-mCherry) and sizes of molecular weight markers (MWM) are indicated. FIG. 26C shows representative differential interference contrast microscopy (left panel) and the corresponding fluorescence image (right panel −25 msec exposure) of a T. thermophila cell expressing the wild type (WT) MLP1-HA-YFP fusion. Arrowheads denote the position of the macronucleus. FIG. 26D shows MPL1-HA-YFP accumulation within macronuclei of live T. thermophila cells expressing an allelic series of fusion proteins WT, (AAA)6-12, and (AAG)12, was visualized by epifluorescence microscopy. Different exposures times are indicated on the right to demonstrate the relative accumulation of each variant. FIG. 26E shows western blot analysis was performed with whole cell lysates made from T. thermophila cells expressing the MLP-HA-YFP fusion proteins. Protein from equivalent cell numbers was loaded in each lane and detected using YFP specific antibody (top panel) and normalized to the nuclear histone species, histone H3 trimethyl-lysine 4 (H3K4m) (bottom panel). Positions of the full-length fusion protein (YFP), normalization control (H3k4m), and sizes of molecular weight markers (MWM) are indicated. Degradation of excess fusion protein is readily apparent as faster migrating species below the full-length MLP1-HA-YFP. FIG. 30F shows steady state levels of fusion gene constructs measured by qRT-PCR. Relative levels of the mRNA for (AAG)12 and (AAA)6-12 are presented as percentage of the wild type (WT) construct mRNA levels. Error bars represent mean±standard deviation values (n=3).

FIG. 27A, FIG. 27B, FIG. 27C, FIG. 27D, FIG. 27E, and FIG. 27F show regulation of reporter gene by polyA tracks in the eukaryotic tissue cultures. FIG. 27A shows fluorescence images of N. benthamiana epidermal cells transiently expressing wild type (WT), (AAG)12 and (AAA)6-12 mCherry constructs. YFP expression was used as a transfection control. (FIG. 27B) Western blot analysis, (FIG. 27C) protein level estimate and (FIG. 27D) mRNA levels for transfected (−) insert control and WT, (AAG)12 and (AAA)6-12 mCherry constructs expressed transiently in N. benthamiana epidermal cells. FIG. 27B shows primary HA-tag antibody was used for detection of HA-mCherry constructs. Phosphinotricin acetyl transferase (BAR) specific antibody was used as a loading and normalization control (FIG. 27C). Levels of mCherry protein from different constructs were derived from detected band intensities normalized for BAR accumulation detected in the same sample. Error bars represent mean values±standard error from biological replicates (n=8). FIG. 27D shows mRNA levels for different mCherry constructs were calculated as cycle threshold (Ct) values and normalized to BAR gene mRNA values. Error bars represent mean values±standard error from biological replicates (n=3). FIG. 27E shows western blot analysis of transient mCherry constructs expression in HeLa cells. WT, 12LysAAG ((AAG)12) and 6-12LysAAA ((AAA)6-12) mCherry proteins were detected using HA-tag specific primary antibody. β-actin was used as a loading control and was detected using specific antibody. Positions of the fusion protein (HA-mCherry), normalization control (β-actin) and sizes of molecular weight markers (MWM) are indicated. FIG. 27F shows quantification of the mCherry protein levels from detected western blot intensities. Levels of mCherry were normalized to β-actin band intensities and represented as a percentage of the wild type construct values.

FIG. 28A, FIG. 28B, FIG. 28C, and FIG. 28D show PolyA tracks regulate mCherry reporter gene expression in different organs of D. melanogaster. FIG. 28A shows diagram of third instar fruit fly larva showing approximate location of salivary glands (SG, blue), central nervous system (CNS, green) and proventriculus (PV, red). Fluorescence imaging of formaldehyde fixed SG (FIG. 28B), CNS (FIG. 28C) and PV (FIG. 28D), dissected from larvae expressing wild type (WT), (AAG)12 and (AAA)6-12 mCherry constructs. mCherry and GFP indicate images acquired by selective fluorescence filter setting. Overlay of mCherry and GFP fluorescence is shown in the merged panel.

FIG. 29A, FIG. 29B, and FIG. 29C show PolyA tracks regulate mCherry reporter expression independently of the promoter strength. FIG. 29A shows western blot analysis of the cell lysates from T-Rex HEK293 stable cell lines expressing doxycycline (Dox) inducible wild type (HA-mCherry) and 12LysAAA insertion construct (HA-(AAA)12-mCherry) from a single locus. Dox concentration in the media was varied from 0 to 0.1 μg/ml. Constitutively expressed δ-tubulin was used as a loading control and was detected using specific antibody. Positions of the fusion protein (HA-mCherry), normalization control (δ-tubulin) and sizes of molecular weight markers (MWM) are indicated. FIG. 29B shows quantification of the mCherry protein levels from detected western blot intensities. Levels of mCherry were normalized to δ-tubulin band intensities and represented as a percentage of the wild type construct values. Numbers indicate concentration of Dox in the media. FIG. 29C shows steady state mRNA levels of the 12LysAAA insertion construct ((AAA)12) measured by qRT-PCR. Relative levels of the mRNA for (AAA)12 are presented as percentage of the wild type (WT) construct mRNA levels. Error bars represent mean±standard deviation values (n=3). Numbers indicate final concentration of Dox in the media.

FIG. 30A and FIG. 30B show regulation of drug resistance and metabolic survival by insertion of polyA track tags in genes from E. coli and S. cerviseae. FIG. 30A shows survival of E. coli cells expressing wildtype (WT), 10LysAAG ((AAG)10) and 3-10LysAAA (AAA)3-10 chloramphenicol acetyltransferase (CAT) constructs on chloramphenicol (CAM) selective media. Pulse induced E. coli cells, expressing different CAT constructs, were plated on selective antibiotic plates with varying amounts of CAM in the media (0-100 mg/ml). Two independent clones were assessed for each construct. E. coli colonies were imaged 16 hours after plating. FIG. 30B shows assays for ADE1 gene regulation by polyA tracks ((AAA)6-12). Ability of S. cerevisiae ade1Δ cells to produce sufficient levels of functional Ade1 protein were assayed by reintroduction of single copy vector with wild type (WT), 12LysAAG ((AAG)12) and 6-12LysAAA ((AAA)6-12) Ade1 construct. Empty vector (EV) served as a negative control. Yeast colonies show diferential red coloration, on the selective SD-Ura media, which is proportional to the activity of Ade1 protein. Adenine dropout media (SD-Ade) selects for yeast cells expressing sufficient amounts of active Ade1 protein. Dilutions of the yeast cultures showing relative survival and growth are indicated.

FIG. 31 shows a diagram of a mCherry expression construct used in E. coli. Position of the inducible arabinose promoter (pBAD), Thioredoxin (Trx), double HA-tag (HA), insertion sequence (X) and fluorescent reporter (mCherry) are indicated. Examples of WT, LysAAG and LysAAA insertions and the resulting protein and DNA sequences of reporter constructs are shown.

FIG. 32 shows a diagram of a mCherry expression construct used in T. thermophila. Position of the inducible metallothionein promoter (MTT1), Macronucleus-Localized Protein 1 (MLP1), double HA-tag (HA) and fluorescent reporter (eYFP) are indicated. Red box designates the position of in frame inserted polyA tracks and 12 LysAAG sequences. WT construct contains no insertions at this position.

FIG. 33 shows diagram of mCherry and YFP expression constructs used in N. benthamiana. Position of the mannopine synthase promoter (MAS-P), the cauliflower mosaic virus 35S promoter and its upstream enhancer (35S), phosphinotricin acetyl transferase (BAR, herbicide resistance gene for selection of transgenic plants), double HA-tag (HA) and fluorescent reporters, mCherry and YFP, are indicated. Red box designates the position of in frame inserted polyA tracks and 12 LysAAG sequences. WT construct contains no insertions at this position.

FIG. 34 shows diagram of mCherry and GFP expression constructs used in D. melanogaster. Position of the heat shock protein 70 promoter (hsp70), upstream activating sequences (UAS, GAL4 DNA binding sequence), double HA-tag (HA) and fluorescent reporters, mCherry and GFP, are indicated. Red box designates the position of in frame inserted polyA tracks and 12 LysAAG sequences. WT construct contains no insertions at this position. Tub-GAL4 driver line used for the expression of mCherry and GFP was derived from BSC42734.

FIG. 35A, FIG. 35B, and FIG. 35C show quantification of mCherry fluorescence in D. melanogaster Salivary Glands (SG), Central Nervous System (CNS), and Proventriculus (PV). Normalized mCherry fluorescence intensity of WT, 12 LysAAG and 6-12 LysAAA in D. melanogaster SG (FIG. 35A), CNS (FIG. 35B) and PV (FIG. 35C). GFP fluorescence was excited by a 488 nm laser and mCherry by a 561 nm laser. All microscopy parameters were constant between tissues, except master gain which was set as follows: SG—488 nm laser master gain was 509, 561 nm laser was 560, CNS—488 nm laser master gain was 625, 561 nm laser was 720, and PV—488 nm laser master gain was 618, 561 nm laser was 616. Fluorescence intensity was measured as an average intensity from each tissue image (Zen 9 software) and plotted as a ratio of mCherry to GFP intensity. Box plots indicate median intensity ratio per construct (n≥5).

FIG. 36 shows western blot analysis and quantification of mCherry protein from third instar D. melanogaster larvae. Five third instar fruit fly larvae expressing either WT, 12 LysAAG or 6-12LysAAA constructs were frozen, homogenized, sonicated and lysed in SDS sample buffer. Equal amounts of lysate were analyzed by SDS-PAGE followed by western blot transfer. mCherry protein was detected using HA-tag antibody (Santa Cruz Biotechlogy Inc) and relative amounts were calculated based on the GFP expression control. GFP protein was detected using GFP specific antibody (Clontech). Relative amounts of mCherry expression are shown as percentage of WT-mCherry expression.

FIG. 37 shows mCherry mRNA abundance in whole third instar D. melanogaster larvae measured by RT-qPCR. Five third instar fruit fly larvae expressing either WT, 12 LysAAG or 6-12LysAAA constructs were frozen, homogenized, and lysed in RiboZol (Ambion). mCherry RNA abundance was measured by RT-qPCR. Relative amounts of mCherry mRNA were normalized to levels of Elongation Factor 1 alpha-100 (EF1) and shown as percentage of WT-mCherry levels. Error bars indicate mean±standard.

FIG. 38A and FIG. 38B show a diagram of mCherry expression constructs and their transcriptional activation in Flp-InTM T-RExTM 293 stable cell lines. FIG. 38A shows scheme of genetic loci expressing WT (HA-mCherry) and 12LysAAA insertion construct (HA-12LysAAA-mCherry) in stable Flp-InTM T-RexTM 293 cell lines. Position of the SV40 promoter (SV40), hygromycin B phosphotransferase (Hygromycin), antibiotic resistance gene for selection of single insertion constructs), doxycyclin-inducible CMV promoter (CMV 2×TetO2), double HA-tag (HA) and fluorescent reporter (mCherry) are indicated. Red box designates the position of in frame inserted 12 LysAAA sequence. WT construct contains no insertions at this position. FIG. 38B shows relative folds of transcriptional activation for WT and 12LysAAA mCherry loci were calculated from mRNA levels for each construct at different levels of induction by doxycycline (Dox, 0.001-0.1 μg/ml). RT-qPCR data for each construct was normalized to the mRNA levels of constitutively expressed hygromycin B phosphotransferase gene. Fold induction was calculated over the non-induced samples for each construct separately. Error bars indicate mean±standard deviation.

FIG. 39 shows diagram of human beta globin delta chain (HBD) expression constructs in Flp-InTM T-RExTM 293 stable cell lines. Scheme of genetic loci expressing WT-HBD and HBD-6LysAAA constructs in stable Flp-InTM T-RExTM 293 cell lines. Position of the SV40 promoter (SV40), hygromycin B phosphotransferase (Hygromycin), antibiotic resistance gene for selection of single insertion constructs), doxycyclin-inducible CMV promoter (CMV 2×TetO2), double HA-tag (HA) and HBD reporter (mCherry) are indicated. Red box designates the position of in frame inserted 6 LysAAA sequence. WT construct contains no insertions at this position.

FIG. 40 shows western blot analysis of HBD protein abundance during Dox induction. Western blot analysis of the cell lysates from Flp-InTM T-RExTM 293 stable cell lines expressing doxycycline (Dox) inducible wild type (WT-HBD) and 6 LysAAA insertion construct (HBD-6LysAAA) from a single locus. Dox concentration in the media was varied from 0.0 to 1 μg/ml. Constitutively expressed β-actin (Actin) was used as a loading control and was detected using specific antibody. Positions of the HA-tagged HBD protein (HA-HBD), normalization control (β-actin) and molecular weight marker (MWM) are indicated.

FIG. 41 shows ratio of WT-HBD and HBD-6LysAAA mRNA abundance from Flp-InTM T-RExTM 293 stable cell lines. Steady state mRNA levels of the 6LysAAA insertion construct (HBD-6LysAAA) measured by qRT-PCR. Relative levels of the mRNA for HBD-6LysAAA are presented as percentage of the wild type HBD (WT-HBD) construct mRNA levels. Error bars represent mean±standard deviation values (n=3). Numbers indicate final concentration of Dox in the media.

FIG. 42 shows diagram of chloramphenicol acetyltransferase (CAT) expression construct used in E. coli. Position of the inducible arabinose promoter (pBAD), Thioredoxin (Trx), double HA-tag (HA), insertion sequences (10 LysAAG and polyA track (3-10LysAAA) and reporter gene (CAT) are indicated.

FIG. 43 shows expression of arabinose-inducible fusion Thioredoxin-HA-CAT constructs in E. coli. Western blot analysis of the lysates from E. coli cells expressing arabinose-inducible wild type Trx-HA-CAT (WT), 10 LysAAG (AAG10) and 3-10 LysAAA insertion constructs (AAA3-10). Cells were induced with 0.5% (w/v) of arabinose in the media for 30 minutes. Equal number of cells were harvested, lysed in SDS sample buffer and loaded on SDS-PAGE gel. Trx-HA-CAT fusion proteins were detected using HA-tag specific antibody. Positions of the Trx-HA-CAT proteins and molecular weight marker (MWM) are indicated. NI represents negative control; WT construct without induction.

FIG. 44A and FIG. 44B shows a diagram of N-succinyl-5-aminoimidazole-4-carboxamide ribotide synthetase (ADE1) construct and expression of ADE1 constructs in S. cerevisiae. FIG. 44A shows position of the orotidine 5′-phosphate decarboxylase promoter and and gene (ura3 and URA3, respectively), ADE1 promoter and gene (ade1 and ADE1, respectively) and FLAG-tag (FLAG) are indicated. Red box (insert) designates the position of in frame inserted 12 LysAAG and 6-12 LysAAA sequences. WT construct contains no insertions at this position. FIG. 44B shows dot blot of yeast cell lysates expressing FLAG-tagged WT, 12 LysAAG and 6-12 LysAAA ADE1 protein from endogenous ade1 promoter. ADE1 protein was detected using anti-Flag (Sigma) antibody. 20 μg of total protein was spotted onto a nitrocellulose membrane for each construct. Ponceau S staining is used as loading control.

FIG. 45A, FIG. 45B, FIG. 45C, and FIG. 45D. Quantification of mCherry fluorescence with modified polyA track sequences. PolyA tracks designed with flanking XAA and AAY codons, where X and Y denote C/G or T/C/G nucleotides respectively, were inserted into the mCherry reporter. The number of lysine residues (K) and adenine residues (A) are noted as well as the two amino acids flanking lysine. The nucleotide and amino acid sequence for K2/A9 (AN) are SEQ ID NO: 91 and 92, respectively. The nucleotide and amino acid sequence for K3/A9 (AS) are SEQ ID NO: 93 and 94, respectively. The nucleotide and amino acid sequence for K2/A10 (QN) are SEQ ID NO: 95 and 96, respectively. The nucleotide and amino acid sequence for K3/A10 (EV) are SEQ ID NO: 97 and 98, respectively. The nucleotide and amino acid sequence for K3/A10 (QV) are SEQ ID NO: 99 and 100, respectively. The nucleotide and amino acid sequence for K3/A11 (AN) are SEQ ID NO: 101 and 102, respectively. The nucleotide and amino acid sequence for K4/A11 (AV) are SEQ ID NO: 103 and 104, respectively. (FIG. 45A). Normalized mCherry fluorescence intensity. (FIG. 45B). PolyA tracks with non-lysine codons interrupting the consecutive AAA codons were inserted into the mCherry reporter. The number of adenosine residues and interrupting codon and the protein sequences are indicated. The nucleic acid sequences for 33As, 15A(CTG)15A, 15A(TAC)15A, 15A(CCC)15A, and 30As are SEQ ID NO: 105, 106, 107, 108, and 109, respectively. (FIG. 45C). Normalized mCherry fluorescence intensity. Error bars represent standard deviation from three different colonies (FIG. 45B and FIG. 45D).

FIG. 46A and FIG. 46B. Illumina sequencing of polyA track genomic insertion. Approximately 30 generations after insertion of HA-(AAA)12-mCherry, genomic DNA was sequenced to examine mutation rate of long PolyA tracks. The fraction of sequencing reads which contain a polyA track vs reads that do not are shown for both genomic DNA and plasmid DNA (FIG. 46A). The non-polyA species of reads from genomic DNA are shown. The nucleic acid sequence shown is SEQ ID NO: 110 (FIG. 46B).

FIG. 47 . Image of the full western blot used in FIG. 26B. Degradation of frameshifted product TRX-HA is indicated. Orientation of the gel is as in the original figure.

FIG. 48A and FIG. 48B Eight biological replicas for experiment represented in FIG. 27B. Loading of samples is in the same order as in the original figure for both mCherry and BAR (BASTA) western blots.

FIG. 49A and FIG. 49B. Complete image of the western blot used in FIG. 27E. Loading and orientation of the western blot is the same as in the original figure. Samples from two biological replicas (FIG. 49A and FIG. 49B) are shown on this image. Replica of FIG. 49A is used for representation in the main figure.

FIG. 50 . Image of the full western blot represented FIG. 29A. Low molecular weight band for degradation product (reacting with HA-antibody) and unspecific high molecular band (reacting with δ-tubulin antibody) are visible on the image. Orientation of the gel is the same as in the original figure.

FIG. 51 . Original plates for the experiments described in FIG. 30A. Two colonies for each construct are excised from the plates to make the final figure.

DETAILED DESCRIPTION OF THE INVENTION

The disclosure provides a method for the translational control of gene expression in cells (e.g., eukaryotic and bacterial cells). In broad terms, the disclosure is based on polyA-triggered ribosome stalling and frameshifting leading to mRNA degradation and an alteration of protein output. The disclosure involves inserting a series of protein sequence tags that differ by several codons to allow tunable amounts of translation, and thus protein output in cells. Control of protein production can be further modulated by differential localization of such sequence tags (e.g. N- or C-terminal) as well as through proteasome and non-sense mediated decay (NMD) inhibition.

Aspects of the disclosure allow for control of protein production at the level of translation based on the insertion into genes of interest of predefined lengths of tagging sequences encoding poly-lysine with iterated AAA and/or AAG codons. These strings of codons induce site-specific cleavage of the mRNA, likely through stalling and frameshifting of the ribosome, as well as inhibition of endogenous stalling and frameshifting of the ribosome, respectively. As such, this system allows differential control of protein expression based on single or multiple base changes within a polylysine track situated within a coding sequence. A wide range of protein output can be achieved by inserting a variety of polyA (e.g., synonymous G-A lysine mutations) and disrupted polyA sequences (e.g., synonymous A-G lysine mutations) within an ORF of a gene.

The presently disclosed subject matter can be used for a variety of research, diagnostic, and/or therapeutic applications for which tunable regulation of protein expression in cells is desired. In one example, the presently disclosed subject matter can be used to achieve site specific mRNA cleavage triggered by a ribosome translating a polynucleotide comprising a polylysine track comprising at least one AAA lysine codon in its coding sequence. In another example, the presently disclosed subject matter involves peptidyl-tRNA drop off on polyA sequences in eukaryotes, archaea, and bacteria. In yet another example, the presently disclosed subject matter can be used to achieve differential expression of recombinant proteins based on single or multiple base changes inside of a polynucleotide tag sequence comprising at least one AAA lysine codon and/or at least one AAG lysine codon, or at least one polylysine track comprising such lysine codons. In a further example, the presently disclosed subject matter provides different sequence tags that specify differential effects on protein output in bacterial, archaeal, and eukaryoic cells.

In sum, the presently disclosed subject matter can be used for the regulation of protein translation in eukaryotic, archaeal, and bacterial systems, the tunable down regulation of essential cellular genes, the controlled expression of proteins and analysis of these effects on cell homeostasis, assays for translational control at various steps of the translation cycle, and the estimation of mRNA translation and turnover, among other uses.

I. METHODS FOR MODULATING THE LEVEL OF EXPRESSION OF POLYPEPTIDES IN CELLS

In an aspect, the presently disclosed subject matter provides a method for modulating the level of expression of a polypeptide in a cell, the method comprising modulating the amount of consecutive adenine (A) nucleotides in at least one lysine codon in an open reading frame of a polynucleotide sequence encoding the polypeptide in the cell, thereby modulating the level of expression of the polypeptide in the cell.

As used herein, “modulating” broadly means to cause or facilitate a qualitative or quantitative change, alteration, or modification in a molecule, a process, pathway, or phenomenon of interest. As used herein, “expression” refers to the process by which a polynucleotide is transcribed from a DNA template (such as into an mRNA or other RNA transcript) and/or the process by which a transcribed mRNA is subsequently translated into peptides, polypeptides, or proteins. Transcripts and encoded polypeptides may be collectively referred to as “gene product.” If the polynucleotide is derived from genomic DNA, expression may include splicing of the mRNA in a cell.

A “gene,” as used herein, refers to a polynucleotide containing at least one open reading frame that is capable of encoding a particular protein after being transcribed and translated. As used herein, a “gene product” is the biochemical material, either RNA or protein, resulting from expression of a gene. A measurement of the amount of gene product is sometimes used to infer how active a gene is. As used herein, “gene expression” is the process by which information from a gene is used in the synthesis of a functional gene product. As used herein, a “reporter gene” refers to a gene that produces a gene product that is easily detected. Examples of reporter genes include, but are not limited to, bioluminescent, fluorescent, computed tomography (CT), magnetic resonance imaging (MRI), positron emission tomography (PET), single-photon emission computed tomography (SPECT) reporter genes, and the like. In some aspects, the reporter gene is a bioluminescent reporter gene (e.g., firefly luciferase). In some aspects, the reporter gene is a fluorescent reporter gene (e.g., a fluorescent protein (GFP, mCherry, etc.).

The terms “polynucleotide”, “polynucleotide sequence”, “nucleotide sequence”, “nucleic acid” and “oligonucleotide” are used interchangeably. They refer to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Polynucleotides may have any three dimensional structure, and may perform any function, known or unknown. The following are non-limiting examples of polynucleotides: coding or non-coding regions of a gene or gene fragment, loci (locus) defined from linkage analysis, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, short interfering RNA (siRNA), short-hairpin RNA (shRNA), micro-RNA (miRNA), ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers. A polynucleotide may comprise one or more modified nucleotides, such as methylated nucleotides and nucleotide analogs. If present, modifications to the nucleotide structure may be imparted before or after assembly of the polymer. The sequence of nucleotides may be interrupted by non-nucleotide components. A polynucleotide may be further modified after polymerization, such as by conjugation with a labeling component.

The terms “polypeptide,” “peptide” and “protein” are used interchangeably herein to refer to polymers of amino acids of any length. The polymer may be linear or branched, it may comprise modified amino acids, and it may be interrupted by non amino acids. The terms also encompass an amino acid polymer that has been modified; non-limiting examples of such modifications include disulfide bond formation, glycosylation, lipidation, acetylation, phosphorylation, or any other manipulation, such as conjugation with a labeling component. As used herein the term “amino acid” includes natural and/or unnatural or synthetic amino acids, including glycine and both the D or L optical isomers, and amino acid analogs and peptidomimetics.

As used herein, “modulating the level of expression” refers to causing or facilitating a qualitative or quantitative change, alteration, or modification in the amount of at least one polypeptide produced in a cell as a result of translation of at least one polynucleotide sequence (e.g., mRNA) encoding such at least one polypeptide. The phrase “modulating the amount of consecutive A nucleotides” means changing the linear sequence of nucleotides that are linked together by phosphodiester bonds in at least one polynucleotide sequence encoding at least one polypeptide of interest to be expressed in a cell a way that increases or decreases the number of contiguous A nucleotides in a targeted region of such polynucleotide sequence.

The presently disclosed subject matter demonstrates that a synonymous lysine mutation consisting of a single AAG-to-AAA codon in a polyA or polylysine track of a nucleic acid sequence (e.g., gene or mRNA) encoding a protein of interest decreases expression of the protein and mRNA stability. Conversely, the presently disclosed subject matter demonstrates that a synonymous lysine mutation consisting of a single AAA-to-AAG codon in a polyA or polylysine track of a nucleic acid sequence (e.g., gene or mRNA) encoding a protein of interest increases expression of the protein and mRNA stability. Put differently, increasing the length of consecutive A nucleotides, for example, by changing selected AAG lysine codons to AAA lysine codons reduces protein expression and mRNA stability, whereas decreasing the length of consecutive A nucleotides, for example, by changing selected AAA lysine codons to AAG lysine codons increases protein expression and mRNA stability.

Accordingly, some aspects of the presently disclosed subject matter contemplate methods for decreasing the level of expression of a polypeptide in a cell, for example, by increasing the amount of consecutive A nucleotides in at least one lysine codon in an open reading frame of a polynucleotide sequence encoding at least one polypeptide in at least one cell.

The terms “decrease”, “reduced”, “reduction”, “decrease” or “inhibit” are all used herein generally to mean a decrease by a statistically significant amount. However, for avoidance of doubt, “reduced”, “reduction”, “decrease” or “inhibit” means a decrease by at least 10% as compared to a reference level, for example a decrease by at least about 20%, or at least about 30%, or at least about 40%, or at least about 50%, or at least about 60%, or at least about 70%, or at least about 80%, or at least about 90%, where the decrease is less than 100%. In one embodiment, the decrease includes a 100% decrease (e.g. absent level as compared to a reference sample), or any decrease between 10-100% as compared to a reference level.

In some embodiments, modulating the amount of consecutive A nucleotides in at least one lysine codon comprises increasing the amount of consecutive A nucleotides in at least one AAG lysine codon in the open reading frame of the polynucleotide sequence encoding the polypeptide in a cell, thereby decreasing the level of expression of the polypeptide in the cell. In the contexts of decreasing the level of expression of a polypeptide in a cell, the methods contemplated herein can decrease protein translation and mRNA stability by at least about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80, 90%, or as much as 100% as compared to a reference level (e.g., an objective measure of the level of expression of at least one polypeptide in a cell employing the method compared to the level of expression of at least one polypeptide in the cell in the absence of employing the method).

The presently disclosed subject matter contemplates using any technique available to the skilled artisan for increasing the amount of consecutive A nucleotides in at least one AAG lysine codon in an open reading frame of a polynucleotide sequence encoding at least one polypeptide in at least one cell.

In some embodiments, increasing the amount of consecutive A nucleotides in the at least one lysine codon comprises introducing at least one synonymous G to A nucleotide mutation into at least one AAG lysine codon. As used herein, “synonymous” in the context of a “nucleotide mutation” refers to a change in the nucleotide of a codon which does not alter the amino acid encoded by such codon. To introduce at least one synonymous G to A nucleotide mutation into at least one AAG lysine codon in an open reading frame of at least one polyucleotide sequence, at least one AAG lysine codon must be identified in the open reading frame. Methods of identifying at least one AAG lysine codon in an open reading frame of at least one polynucleotide encoding at least one polypeptide of interest are well known to the skilled artisan. For example, the position of at least one AAG lysine codon in an open reading frame of at least one polynucleotide encoding at least one polypeptide can be determined using publicly available sequence databases and bioinformatics tools (e.g., BLAST searching, mRNA mapping, etc.). When the position of at least one AAG lysine codon in an open reading frame of at least one polynucleotide encoding at least one polypeptide is determined, at least one synonymous G to A nucleotide mutation can be introduced into such at least one AAG lysine codon, for example, using site directed mutagenesis. It should be appreciated, however, it is the number of consecutive A nucleotides that controls the levels of protein expression and mRNA stability. As such, it may be advantageous to identify at least one AAG lysine codon that is flanked by an upstream codon that ends with an A nucleotide (e.g., UUA (Leu), AUA (Ile), GUA (Val), UCA (Ser), CCA (Pro), ACA (Thr), GCA (Ala), UAU (Tyr), CAA (Gln), AAA (Lys), GAA (Glu), CGA (Arg), AGA (Arg), and GGA (Gly)) and/or is flanked by a downstream codon that begins with an A nucleotide (e.g., AUU (Ile), AUC (Ile), AUA (Ile), AUG (Met), ACU (Thr), ACC (Thr), ACA (Thr), ACG (Thr), AAU (Asn), AAC (Asn), AAA (Lys), AAG (Lys), AGU (Ser), AGC (Ser), AGA (Arg), and AGG (Arg)) for introduction of at least one synonymous G to A nucleotide mutation, for example, to increase the number of consecutive A nucleotides in the polynucleotide sequence with the resultant decrease in the level of expression of at least one polypeptide encoded by such polynucleotide sequence. Accordingly, in some embodiments, the method comprises introducing at least one synonymous G to A nucleotide mutation into at least one AAG lysine codon that is flanked by an upstream codon that ends with an A nucleotide and/or is flanked by a downstream codon that begins with an A nucleotide.

Generally, it is believed that the greater the increase in the number of consecutive A nucleotides in at least one polynucleotide sequence encoding at least one polypeptide, the greater the decrease will be in the level of expression of the at least one polypeptide. The skilled artisan will appreciate that the increase in the number of consecutive A nucleotides introduced into at least one polynucleotide sequence in this manner will be limited by the number of AAG lysine codons in the open reading frame of such polynucleotide sequence, as well as those AAG lysine codons that are flanked by upstream codons ending with A nucleotides and/or are flanked by downstream codons beginning with A nucleotides.

In some embodiments, at least one synonymous G to A nucleotide mutation is introduced into at least one AAG lysine codon in an open reading frame of at least one polynucleotide sequence. In some embodiments, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least 11, at least 12, or at least n synonymous G to A nucleotide mutations (where n is a positive integer greater than or equal to 13 and less than or equal to the number of AAG lysine codons in a particular polynucleotide sequence) are introduced into at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least 11, at least 12, or at least n AAG lysine codons (where n is a positive integer greater than or equal to 13 and less than or equal to the number of AAG lysine codons in a particular polynucleotide sequence) in an open reading frame of at least one polynucleotide sequence.

In other embodiments, increasing the amount of consecutive A nucleotides in the at least one lysine codon comprises inserting at least one AAA lysine codon into the open reading frame of the polynucleotide sequence encoding the polypeptide in the cell. It should be appreciated that any amount of at least one AAA lysine codons can be inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide in a cell. In general, the greater the amount of consecutive A nucleotides inserted into an open reading frame of at least one polynucleotide sequence, the greater the decrease in the level of expression of at least one polypeptide encoded by the at least one polynucleotide sequence. In this way, levels of expression of at least one polypeptide can be controlled in a cell. In some embodiments, at least one (AAA) lysine codon is inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest in a cell. In some embodiments, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least eleven, at least 12, or at least n AAA lysine codons ((AAA)n) (where n is a positive integer greater than or equal to 13) are inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest in a cell. In some embodiments, at least one, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least 11, at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18, at least 19, at least 20, at least 21, at least 22, at least 23, at least 24, at least 25, at least 26, at least 27, at least 28, at least 29, at least 30, at least 31, at least 32, at least 33, at least 34, at least 35, at least 36, or at least n A nucleotides ((A)n) (where n is a positive integer greater than or equal to 37) are inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest in a cell.

The AAA lysine codons and/or consecutive A nucleotides can be inserted in the form of one or more polynucleotide sequence tags designed for tunable expression of at least one polypeptide in a cell. In some embodiments, at least one polyA polynucleotide sequence tag can be inserted in an open reading frame, for example, in between an upstream codon ending with an A nucleotide and a downstream codon beginning with an A nucleotide. In some embodiments, two or more polyA polynucleotide sequence tags can be inserted adjacent to each other or spaced apart by intervening polynucleotides sequences in the open reading frame.

The presently disclosed subject matter contemplates insertion of at least one AAA lysine codon, a consecutive number of A nucleotides, and/or a polyA polynucleotide sequence tag into any portion of an open reading frame in at least one polynucleotide encoding at least one polypeptide in a cell. In some embodiments, at least one AAA lysine codon is inserted into a coding sequence of the open reading frame. In some embodiments, two or more polyA polynucleotide sequence tags are inserted into a coding sequence of at least one polypeptide. In some embodiments, at least one AAA lysine codon is inserted into a 5′ untranslated region (UTR) of at least one polynucleotide encoding a polypeptide in a cell. In some embodiments, a polyA polynucleotide sequence tag is inserted into a 5′ UTR of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAA lysine codon is inserted into an exon of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, a polyA polynucleotide sequence tag is inserted into an exon of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAA lysine codon is inserted into an exon/intron boundary of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, a polyA polynucleotide sequence tag is inserted into an exon/intron boundary of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAA lysine codon is inserted into an intron of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, a polyA polynucleotide sequence tag is inserted into an intron of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAA lysine codon is inserted into a 3′ UTR of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, a polyA polynucleotide sequence tag is inserted into a 3′ UTR of at least one polynucleotide encoding a polypeptide of interest.

In some embodiments, at least one polyA polynucleotide sequence tag comprises one or more AAG lysine codons, for example, for tunable expression of at least one polypeptide of interest encoded by at least one polynucleotide into which the at least one polyA polynucleotide sequence tag is inserted. Examples of such polyA nucleotide sequence tags include at least one AAA lysine codon preceded or followed by at least one AAG lysine codon, a first AAA lysine codon and a second AAA lysine codon flanking an AAG lysine codon, alternating AAG and AAA lysine codons (e.g., (AAG-AAA)n (where n is a positive integer greater than or equal to 1), triple repeats comprising combinations of AAG and AAA lysine codons (e.g., (AAA-AAG-AAA)n, (AAG-AAA-AAA)n, (AAA-AAA-AAG)n, where each n is a positive integer greater than or equal to 1), quadruple repeats, etc. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In some embodiments, n is 6. In some embodiments, n is 6. In some embodiments, n is 8. In some embodiments, n is 9. In some embodiments, n is 10. In some embodiments, n is 11. In some embodiments, n is 12.

Some aspects of the presently disclosed subject matter contemplate methods for increasing the level of expression of a polypeptides in a cell, for example, by decreasing the amount of consecutive A nucleotides in at least one lysine codon in an open reading frame of a polynucleotide sequence encoding at least one polypeptide in at least one cell.

The terms “increased”, ‘increase”, “enhance” or “activate” are all used herein to generally mean an increase by a statically significant amount; for the avoidance of any doubt, the terms “increased”, “increase”, “enhance” or “activate” means an increase of at least 10% as compared to a reference level, for example an increase of at least about 20%, or at least about 30%, or at least about 40%, or at least about 50%, or at least about 60%, or at least about 70%, or at least about 80%, or at least about 90% or up to and including a 100% increase or any increase between 10-100% as compared to a reference level, or at least about a 2-fold, or at least about a 3-fold, or at least about a 4-fold, or at least about a 5-fold or at least about a 10-fold increase, or any increase between 2-fold and 10-fold or greater as compared to a reference level.

In some embodiments, modulating the amount of consecutive A nucleotides in the at least one lysine codon comprises decreasing the amount of consecutive A nucleotides in the at least one AAA lysine codon in an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest in a cell, thereby increasing the level of expression of the polypeptide in the cell. In the contexts of increasing the level of expression of a polypeptide in a cell, the methods contemplated herein can increase protein translation and mRNA stability, by at least about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80, 90%, or as much as 100%, at least about a 2-fold, or at least about a 3-fold, or at least about a 4-fold, or at least about a 5-fold or at least about a 10-fold increase, or any increase between 2-fold and 10-fold or greater as compared to a reference level (e.g., an objective measure of the level of expression of at least one polypeptide in a cell employing the method compared to the level of expression of at least one polypeptide in the cell in the absence of employing the method).

The presently disclosed subject matter contemplates using any technique available to the skilled artisan for decreasing the amount of consecutive A nucleotides in at least one lysine codon in an open reading frame of a polynucleotide sequence encoding at least one polypeptide of interest. In some embodiments, decreasing the amount of consecutive A nucleotides in at least one lysine codon comprises introducing at least one synonymous A to G nucleotide mutation into the at least one AAA lysine codon. To introduce at least one synonymous A to G nucleotide mutation into at least one AAA lysine codon in an open reading frame of at least one polyucleotide sequence, at least one AAA lysine codon must be identified in the open reading frame using methods which are well known to the skilled artisan. When the position of at least one AAA lysine codon in an open reading frame of at least one polynucleotide encoding at least one polypeptide is determined, at least one synonymous A to G nucleotide mutation can be introduced into such at least one AAA lysine codon, for example, using site directed mutagenesis. It should be appreciated, however, it is the number of consecutive A nucleotides that controls the levels of protein expression and mRNA stability. As such, it may be advantageous to identify at least one AAA lysine codon flanked by an upstream codon that ends with an A nucleotide (e.g., UUA (Leu), AUA (Ile), GUA (Val), UCA (Ser), CCA (Pro), ACA (Thr), GCA (Ala), UAU (Tyr), CAA (Gln), AAA (Lys), GAA (Glu), CGA (Arg), AGA (Arg), and GGA (Gly)) and/or flanked by a downstream codon that begins with an A nucleotide (e.g., AUU (Ile), AUC (Ile), AUA (Ile), AUG (Met), ACU (Thr), ACC (Thr), ACA (Thr), ACG (Thr), AAU (Asn), AAC (Asn), AAA (Lys), AAG (Lys), AGU (Ser), AGC (Ser), AGA (Arg), andAGG (Arg)) to introduce at least one synonymous A to G nucleotide mutation into, for example, to decrease the number of consecutive A nucleotides in the polynucleotide sequence with the resultant increase in the level of expression of at least one polypeptide encoded by such polynucleotide sequence. Accordingly, in some embodiments, the method comprises introducing at least one synonymous A to G nucleotide mutation into at least one AAA lysine codon flanked by an upstream codon that ends with an A nucleotide and/or flanked by a downstream codon that begins with an A nucleotide.

Generally, it is believed that the greater the decrease in the number of consecutive A nucleotides in at least one polynucleotide sequence encoding at least one polypeptide of interest, the greater the increase will be in the level of expression of the at least one polypeptide of interest. The skilled artisan will appreciate that the decrease in the number of consecutive A nucleotides in at least one polynucleotide sequence will be limited by the number of consecutive A nucleotides in such sequence, and in particular embodiments by the number of AAA lysine codons in the open reading frame of such polynucleotide sequence.

In some embodiments, at least one synonymous A to G nucleotide mutation is introduced into at least one AAA lysine codon in an open reading frame of at least one polynucleotide sequence encoding a polypeptide of interest. In some embodiments, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least 11, at least 12, or at least n synonymous A to G nucleotide mutations (where n is a positive integer greater than or equal to 13 and less than or equal to the number of AAA lysine codons in a particular polynucleotide sequence) are introduced into at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least 11, at least 12, or at least n AAA lysine codons (where n is a positive integer greater than or equal to 13 and less than or equal to the number of AAA lysine codons in a particular polynucleotide sequence) in an open reading frame of at least one polynucleotide sequence.

In other embodiments, decreasing the amount of consecutive A nucleotides in at least one lysine codon comprises inserting at least one AAG lysine codon into the open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest. It should be appreciated that any amount of at least one AAG lysine codons can be inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest. In general, the greater the amount of AAG lysine codons inserted into an open reading frame of at least one polynucleotide sequence, the greater the increase in the level of expression of at least one polypeptide encoded by the at least one polynucleotide sequence. In this way, levels of expression of at least one polypeptide can be controlled in a cell. In some embodiments, at least one (AAG) lysine codon is inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest. In some embodiments, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, at least 10, at least eleven, at least 12, or at least n AAG lysine codons ((AAG)n) (where n is a positive integer greater than or equal to 13) are inserted into an open reading frame of at least one polynucleotide sequence encoding at least one polypeptide of interest.

The AAG lysine codons can be inserted in the form of one or more poly AAG lysine polynucleotide sequence tags designed for tunable expression of at least one polypeptide in a cell. In some embodiments, at least one polyAAG lysine polynucleotide sequence tag can be inserted in an open reading frame. In some embodiments, two or more polyAAG lysine polynucleotide sequence tags can be inserted in the open reading frame.

The presently disclosed subject matter contemplates insertion of at least one AAG lysine codon, and/or a polyAAG lysine polynucleotide sequence tag into any portion of an open reading frame in at least one polynucleotide encoding at least one polypeptide of interest. In some embodiments, at least one AAG lysine codon is inserted into a coding sequence of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one poly AAG lysine polynucleotide sequence tag is inserted into a coding sequence of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAG lysine codon is inserted into a 5′ untranslated region (UTR) of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, a polyAAG lysine polynucleotide sequence tag is inserted into a 5′ UTR of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAG lysine codon is inserted into an exon/intron boundary of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, a polyAAG lysine polynucleotide sequence tag is inserted into an exon/intron boundary of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAG lysine codon is inserted into an intron of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one polyAAG lysine polynucleotide sequence tag is inserted into an intron of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one AAG lysine codon is inserted into a 3′ UTR of at least one polynucleotide encoding a polypeptide of interest. In some embodiments, at least one polyAAG lysine polynucleotide sequence tag is inserted into a 3′ UTR of at least one polynucleotide encoding a polypeptide of interest.

In some embodiments, at least one polyAAG lysine polynucleotide sequence tag comprises one or more AAA lysine codons, for example, for tunable expression of at least one polypeptide of interest encoded by at least one polynucleotide into which the at least one polyAAG lysine polynucleotide ssequence tag is inserted. Examples of such polyAAG lysine polynucleotide sequence tags include at least one AAG lysine codon preceded or followed by at least one AAA lysine codon, a first AAG lysine codon and a second AAG lysine codon flanking an AAA lysine codon, alternating AAA and AAG lysine codons (e.g., (AAA-AAG)n (where n is a positive integer greater than or equal to 1), triple repeats comprising combinations of AAA and AAG lysine codons (e.g., (AAG-AAA-AAG)n, (AAA-AAG-AAG)n, (AAG-AAG-AAA)n, where each n is a positive integer greater than or equal to 1), quadruple repeats, etc. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In some embodiments, n is 6. In some embodiments, n is 6. In some embodiments, n is 8. In some embodiments, n is 9. In some embodiments, n is 10. In some embodiments, n is 11. In some embodiments, n is 12.

In some embodiments, at least one AAG lysine codon is inserted into at least one polynucleotide sequence for expression at an N-terminus or C-terminus of at least one polypeptide of interest to be expressed in a cell. In some embodiments, at least one polyAAG lysine polynucleotide sequence tag comprises a N-terminus tag. In some embodiments, at least one polyAAG lysine polynucleotide sequence tag comprises a C-terminus tag.

Those skilled in the art will appreciate that the manner in which at least one synonymous lysine mutation (e.g., at least one synonymous A to G nucleotide mutation or at least one synonymous G to A nucleotide mutation) is introduced into at least one lysine codon, the manner in which at least one lysine codon (e.g., at least one AAA lysine codon or at least one AAG lysine codon) is inserted into an open reading frame of at least one polynucleotide sequence enoding a polypeptide of interest, and/or the manner in which at least one polylysine sequence tag (e.g., at least one polyA track or polyA polynucleotide sequence tag or at least one polyAAG lysine track or polyAAG lysine polynucleotide sequence tag) is inserted into an open reading frame of at least one polynucleotide sequence encoding a polypeptide of interest depends on whether at least one polynucleotide encoding at least one polypeptide of interest is an endogenous polynucleotide sequence in a cell, or an exogenous polynucleotide sequence encoding a heterologous protein to be expressed in a cell.

In some embodiments, at least one polynucleotide sequence comprises an endogenous polynucleotide sequence and the step of modulating the amount of consecutive A nucleotides in the at least one lysine codon includes selecting an endogenouous polynucleotide sequence in the cell that comprises at least one lysine codon, and editing the endogenous polynucleotide sequence in the cell. The presently disclosed subject matter contemplates editing endogenous polynucleotide sequences in cells that is available to the skilled artisan. In some embodiments, editing the endogenous polynucleotide sequence in the cell comprises contacting the cell with an engineered nuclease selected from the group consisting of a CRISPR-Cas system, CRISPR-Cpf1 system, a zinc finger nuclease (ZFN), a transcription activator-like effector nuclease (TALEN), and a meganuclease.

In other embodiments, at least one polynucleotide sequence comprises an exogenous polynucleotide sequence and the step of modulating the amount of consecutive A nucleotides in the at least one lysine codon includes providing an expression vector comprising an exogenous polynucleotide sequence comprising at least one AAA lysine codon or at least one AAG lysine codon inserted thereinto operably linked to a promoter that drives expression of the exogenous polynucleotide in the cell, and contacting the cell with the expression vector.

In some embodiments, at least one lysine codon comprises at least one polylysine track selected from the group consisting of AAA lysine codons, AAG lysine codons, and combinations thereof. In some embodiments, at least one polylysine track comprises between 4 and 36 A nucleotides. In some embodiments, at least one polylysine track comprises at least 11 consecutive A nucleotides in at least three consecutive lysine codons.

In some embodiments, exogenouc polynucleotide sequences comprising at least one lysine codon and/or at least one polylysine track, and/or at least one polyA polynucleotide sequence tag and/or at least one polyAAG lysine polynucleotide sequence tag can be synthesized utilizing in vitro transcription methods which are well known to the skilled artisan.

In some embodiments, at least one lysine codon, at least one polyA polynucleotide sequence tag, and/or at least one polylysine track is not a polyA tail. In some embodiments, at least one lysine codon, at least one polyA polynucleotide sequence tag, and/or at least one polylysine (polyA) track is not located in the 3′ UTR or downstream of the 3′ UTR.

II. EXPRESSION VECTORS

Aspects of the presently disclosed subject matter relate to expression vectors for the tunable expression of polypeptides of interest in cells. The presently disclosed expression vectors comprise at least one polynucleotide comprising at least one lysine codon, at least one polylysine track, at least one polyA polynucleotide sequence tag, and/or at least one polyAAG lysine polynucleotide sequence tag.

In general, and throughout this specification, the term “vector” refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. Vectors include, but are not limited to, nucleic acid molecules that are single-stranded, double-stranded, or partially double-stranded; nucleic acid molecules that comprise one or more free ends, no free ends (e.g. circular); nucleic acid molecules that comprise DNA, RNA, or both; and other varieties of polynucleotides known in the art. One type of vector is a “plasmid,” which refers to a circular double stranded DNA loop into which additional DNA segments can be inserted, such as by standard molecular cloning techniques. Another type of vector is a viral vector, wherein virally-derived DNA or RNA sequences are present in the vector for packaging into a virus (e.g. retroviruses, replication defective retroviruses, adenoviruses, replication defective adenoviruses, and adeno-associated viruses). Viral vectors also include polynucleotides carried by a virus for transfection into a host cell.

Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g. bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors are capable of directing the expression of genes to which they are operatively-linked. Such vectors are referred to herein as “expression vectors.” Common expression vectors of utility in recombinant DNA techniques are often in the form of plasmids.

Recombinant expression vectors can comprise a nucleic acid of the presently disclosed subject matter in a form suitable for expression of the nucleic acid in a host cell, which means that the recombinant expression vectors include one or more regulatory elements, which may be selected on the basis of the host cells to be used for expression, that is operatively-linked to the nucleic acid sequence to be expressed.

Within a recombinant expression vector, “operably linked” is intended to mean that the nucleotide sequence of interest is linked to the regulatory element(s) in a manner that allows for expression of the nucleotide sequence (e.g. in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell).

The term “regulatory element” is intended to include promoters, enhancers, internal ribosomal entry sites (IRES), and other expression control elements (e.g. transcription termination signals, such as polyadenylation signals and poly-U sequences). Such regulatory elements are described, for example, in Goeddel (1990) Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. Regulatory elements include those that direct constitutive expression of a nucleotide sequence in many types of host cell and those that direct expression of the nucleotide sequence only in certain host cells (e.g., tissue-specific regulatory sequences). In some embodiments, the promoter is an inducible promoter that is active in response to specific stimuli.

A cell-specific promoter may direct expression primarily in a desired cell of interest, such as muscle cell, a neuron, a skin cell, a blood cell, an immune cell, a liver cell, a pancreatic cell, a spleen cell, etc. In some embodiments, the promoter is a tissue-specific promoter that is active in specific tissues. In some embodiments, the promoter is a tumor-specific promoter that is active specifically in tumor cells. Regulatory elements may also direct expression in a temporal-dependent manner, such as in a cell-cycle dependent or developmental stage-dependent manner, which may or may not also be tissue or cell-type specific.

In some embodiments, a vector comprises one or more pol III promoters, one or more pol II promoters, one or more pol I promoters, or combinations thereof. Examples of pol III promoters include, but are not limited to, U6 and H1 promoters. Examples of pol II promoters include, but are not limited to, the retroviral Rous sarcoma virus (RSV) LTR promoter (optionally with the RSV enhancer), the cytomegalovirus (CMV) promoter (optionally with the CMV enhancer) (e.g., Boshart et al. (1985) Cell 41:521-530), the SV40 promoter, the dihydrofolate reductase promoter, the β-actin promoter, the phosphoglycerol kinase (PGK) promoter, and the EF1α promoter.

Also encompassed by the term “regulatory element” are enhancer elements, such as WPRE; CMV enhancers; the R-U5′ segment in LTR of HTLV-I (Takebe et al. (1988) Mol. Cell. Biol.8:466-472); SV40 enhancer; and the intron sequence between exons 2 and 3 of rabbit β-globin (O'Hare et al. (1981) Proc. Natl. Acad. Sci. USA. 78(3):1527-31). It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression desired, etc. A vector can be introduced into host cells to thereby produce transcripts, proteins, or peptides, including fusion proteins or peptides, encoded by nucleic acids as described herein (e.g., clustered regularly interspersed short palindromic repeats (CRISPR) transcripts, proteins, enzymes, mutant forms thereof, fusion proteins thereof, etc.). Advantageous vectors include lentiviruses and adeno-associated viruses, and types of such vectors can also be selected for targeting particular types of cells.

As used herein the term “wild type” is a term of the art understood by skilled persons and means the typical form of an organism, strain, gene or characteristic as it occurs in nature as distinguished from mutant or variant forms.

As used herein the term “variant” should be taken to mean the exhibition of qualities that have a pattern that deviates from what occurs in nature.

The terms “non-naturally occurring” or “engineered” are used interchangeably and indicate the involvement of the hand of man. The terms, when referring to nucleic acid molecules or polypeptides mean that the nucleic acid molecule or the polypeptide is at least substantially free from at least one other component with which they are naturally associated in nature and as found in nature.

“Complementarity” refers to the ability of a nucleic acid to form hydrogen bond(s) with another nucleic acid sequence by either traditional Watson-Crick or other non-traditional types. A percent complementarity indicates the percentage of residues in a nucleic acid molecule which can form hydrogen bonds (e.g., Watson-Crick base pairing) with a second nucleic acid sequence (e.g., 5, 6, 7, 8, 9, 10 out of 10 being 50%, 60%, 70%, 80%, 90%, and 100% complementary). “Perfectly complementary” means that all the contiguous residues of a nucleic acid sequence will hydrogen bond with the same number of contiguous residues in a second nucleic acid sequence. “Substantially complementary” as used herein refers to a degree of complementarity that is at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%. 97%, 98%, 99%, or 100% over a region of 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 35, 40, 45, 50, or more nucleotides, or refers to two nucleic acids that hybridize under stringent conditions.

As used herein, “stringent conditions” for hybridization refer to conditions under which a nucleic acid having complementarity to a target sequence predominantly hybridizes with the target sequence, and substantially does not hybridize to non-target sequences. Stringent conditions are generally sequence-dependent, and vary depending on a number of factors. In general, the longer the sequence, the higher the temperature at which the sequence specifically hybridizes to its target sequence. Non-limiting examples of stringent conditions are described in detail in Tijssen (1993), Laboratory Techniques In Biochemistry And Molecular Biology-Hybridization With Nucleic Acid Probes Part 1, Second Chapter “Overview of principles of hybridization and the strategy of nucleic acid probe assay”, Elsevier, N.Y.

“Hybridization” refers to a reaction in which one or more polynucleotides react to form a complex that is stabilized via hydrogen bonding between the bases of the nucleotide residues. The hydrogen bonding may occur by Watson Crick base pairing, Hoogstein binding, or in any other sequence specific manner. The complex may comprise two strands forming a duplex structure, three or more strands forming a multi stranded complex, a single self hybridizing strand, or any combination of these. A hybridization reaction may constitute a step in a more extensive process, such as the initiation of PCR, or the cleavage of a polynucleotide by an enzyme. A sequence capable of hybridizing with a given sequence is referred to as the “complement” of the given sequence.

Vectors may be introduced and propagated in a prokaryote. In some embodiments, a prokaryote is used to amplify copies of a vector to be introduced into a eukaryotic cell or as an intermediate vector in the production of a vector to be introduced into a eukaryotic cell (e.g. amplifying a plasmid as part of a viral vector packaging system). In some embodiments, a prokaryote is used to amplify copies of a vector and express one or more nucleic acids, such as to provide a source of one or more proteins for delivery to a host cell or host organism. Expression of proteins in prokaryotes is most often carried out in Escherichia coli with vectors containing constitutive or inducible promoters directing the expression of either fusion or non-fusion proteins.

Fusion vectors add a number of amino acids to a protein encoded therein, such as to the amino terminus of the recombinant protein. Such fusion vectors may serve one or more purposes, such as: (i) to increase expression of recombinant protein; (ii) to increase the solubility of the recombinant protein; and (iii) to aid in the purification of the recombinant protein by acting as a ligand in affinity purification. Often, in fusion expression vectors, a proteolytic cleavage site is introduced at the junction of the fusion moiety and the recombinant protein to enable separation of the recombinant protein from the fusion moiety subsequent to purification of the fusion protein. Such enzymes, and their cognate recognition sequences, include Factor Xa, thrombin and enterokinase. Example fusion expression vectors include pGEX (Pharmacia Biotech Inc; Smith and Johnson (1988) Gene 67: 31-40), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, N.J.) that fuse glutathione S-transferase (GST), maltose E binding protein, or protein A. respectively, to the target recombinant protein.

Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amrann et al. (1988) Gene 69:301-315) and pET 11d (Studier et al. (1990) Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif.).

In some embodiments, a vector is a yeast expression vector. Examples of vectors for expression in yeast Saccharomyces cerivisae include pYepSec1 (Baldari, et al.(1987) EMBO J. 6: 229-234), pMFa (Kuijan and Herskowitz (1982) Cell 30: 933-943), pJRY88 (Schultz et al. (1987) Gene 54: 113-123), pYES2 (Invitrogen Corporation, San Diego, Calif.), and picZ (InVitrogen Corp, San Diego, Calif.).

In some embodiments, a vector is capable of driving expression of one or more sequences in mammalian cells using a mammalian expression vector. Examples of mammalian expression vectors include pCDM8 (Seed (1987) Nature 329: 840) and pMT2PC (Kaufman et al. (1987) EMBO J. 6: 187-195). When used in mammalian cells, the expression vector's control functions are typically provided by one or more regulatory elements. For example, commonly used promoters are derived from polyoma, adenovirus 2, cytomegalovirus, simian virus 40, and others disclosed herein and known in the art. For other suitable expression systems for both prokaryotic and eukaryotic cells see, e.g., Chapters 16 and 17 of Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual. 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y..

In some embodiments, the recombinant mammalian expression vector is capable of directing expression of the nucleic acid preferentially in a particular cell type (e.g., tissue-specific regulatory elements are used to express the nucleic acid). Tissue-specific regulatory elements are known in the art. Non-limiting examples of suitable tissue-specific promoters include the albumin promoter (liver-specific; Pinkert et al. (1987) Genes Dev. 1: 268-277), lymphoid-specific promoters (Calame and Eaton (1988) Adv. Immunol. 43: 235-275), in particular promoters of T cell receptors (Winoto and Baltimore (1989) EMBO J.8: 729-733) and immunoglobulins (Baneiji et al. (1983) Cell 33: 729-740; Queen and Baltimore (1983) Cell 33: 741-748), neuron-specific promoters (e.g., the neurofilament promoter; Byrne and Ruddle (1989) Proc. Natl. Acad. Sci. USA 86: 5473-5477), pancreas-specific promoters (Edlund et al.(1985) Science 230: 912-916), and mammary gland-specific promoters (e.g., milk whey promoter; U.S. Pat. No. 4,873,316 and European Application Publication No. 264,166). Developmentally-regulated promoters are also encompassed, e.g., the murine hox promoters (Kessel and Gruss (1990) Science 249: 374-379) and the α-fetoprotein promoter (Campes and Tilghman (1989) Genes Dev. 3: 537-546).

In some aspects, the presently disclosed subject matter provides an expression vector comprising a cloning site for inserting at least one polynucleotide sequence encoding a polypeptide to be expressed, and at least one polynucleotide tag sequence comprising at least one AAG lysine codon that increases expression of the at least one polynucleotide sequence when the expression vector is introduced into a cell. In some embodiments, at least one polynucleotide tag sequence comprises at least one polylysine track comprising at least two consecutive AAG lysine codons. In some embodiments, at least one polylysine track comprises at least two consecutive AAG lysine codons selected from the group consisting of (AAG)2, (AAG)3, (AAG)6, and (AAG)12. In some embodiments, at least one polylysine track comprises at least n consecutive AAG lysine codons (i.e., (AAG)n), where n is a positive integer greater than or equal to 13.

In some aspects, the presently disclosed subject matter provides an expression vector comprising a cloning site for inserting at least one polynucleotide sequence encoding a polypeptide to be expressed, and at least one polynucleotide tag sequence comprising at least one AAA lysine codon that decreases expression of the at least one polynucleotide sequence when the expression vector is introduced into a cell. In some embodiments, at least one polynucleotide tag sequence comprises at least one polylysine track comprising at least two consecutive AAA lysine codons. wherein the and wherein the at least one polylysine track in b) comprises at least two consecutive AAA lysine codons selected from the group consisting of (AAA)2, (AAA)3, (AAA)6, and (AAA)12. In some embodiments, at least one polylysine track comprises at least n consecutive AAA lysine codons (i.e., (AAA)n), where n is a positive integer greater than or equal to 13.

In some aspects, the presently disclosed subject matter provides an expression vector comprising at least one engineered polynucleotide sequence encoding a polypeptide to be expressed, the at least one engineered polynucleotide sequence comprising at least one engineered synonymous mutation of at least one AAA lysine codon to at least one AAG lysine codon in a coding sequence of the at least one polynucleotide sequence, wherein the synonymous mutation increases expression of the polypeptide to be expressed when the expression vector is introduced into a cell. In some embodiments, at least one engineered polynucleotide sequence comprises at least one polylysine track comprising at least two consecutive lysine codons in the coding sequence. In some embodiments, at least one polylysine track comprises at least two consecutive AAG lysine codons selected from the group consisting of (AAG)2, (AAG)3, (AAG)6, and (AAG)12. In some embodiments, at least one polylysine track comprises at least n consecutive AAG lysine codons (i.e., (AAG)n where n is a positive integer greater than or equal to 13).

In some aspects, the presently disclosed subject matter provides an expression vector comprising at least one engineered polynucleotide sequence encoding a polypeptide to be expressed, the at least one engineered polynucleotide sequence comprising at least one engineered synonymous mutation of at least one AAG lysine codon to at least one AAA lysine codon in a coding sequence of the at least one polynucleotide sequence, wherein the synonymous mutation decreases expression of the polypeptide to be expressed when the expression vector is introduced into a cell.

In some embodiments, at least one engineered polynucleotide sequence comprises at least one polylysine track comprising at least two consecutive lysine codons in the coding sequence. In some embodiments, at least one polylysine track comprises at least two consecutive AAA lysine codons selected from the group consisting of (AAA)2, (AAA)3, (AAA)6, and (AAA)12. In some embodiments, at least one polylysine track comprises at least n consecutive AAA lysine codons (i.e., (AAA)n where n is a positive integer greater than or equal to 13).

In some embodiments, at least one polylysine track comprises at least 11 consecutive A nucleotides in at least three consecutive lysine codons, prior to enginnering the at least one engineered polynucleotide sequence to include the at least one engineered synonymous mutation.

Vectors can be designed for expression of CRISPR transcripts (e.g. nucleic acid transcripts, proteins, or enzymes) in prokaryotic or eukaryotic cells. For example, CRISPR transcripts can be expressed in bacterial cells such as Escherichia coli, insect cells (using baculovirus expression vectors), yeast cells, or mammalian cells. Suitable host cells are discussed further in Goeddel (1990) Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. Alternatively, the recombinant expression vector can be transcribed and translated in vitro, for example using T7 promoter regulatory sequences and T7 polymerase.

In aspects of the presently disclosed subject matter the terms “chimeric RNA”, “chimeric guide RNA”, “guide RNA”, “single guide RNA” and “synthetic guide RNA” are used interchangeably and refer to the polynucleotide sequence comprising the guide sequence. The term “guide sequence” refers to the about 20 bp sequence within the guide RNA that specifies a target sequence and may be used interchangeably with the terms “guide” or “spacer”.

A target sequence may comprise any polynucleotide, such as DNA or RNA polynucleotides. In some embodiments, a target sequence is located in the nucleus or cytoplasm of a cell. In some embodiments, the target sequence may be within an organelle of a eukaryotic cell, for example, mitochondrion or chloroplast. A sequence or template that may be used for recombination into the targeted locus comprising the target sequences is referred to as an “editing template” or “editing polynucleotide” or “editing sequence”. In aspects of the presently disclosed subject matter, an exogenous template polynucleotide may be referred to as an editing template. In an aspect of the presently disclosed subject matter the recombination is homologous recombination.

In some embodiments, a vector comprises one or more insertion sites, such as a restriction endonuclease recognition sequence (also referred to as a “cloning site”). In some embodiments, one or more insertion sites (e.g. about or more than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more insertion sites) are located upstream and/or downstream of one or more sequence elements of one or more vectors

In some embodiments, the degree of complementarity between a guide sequence and its corresponding target sequence, when optimally aligned using a suitable alignment algorithm, is about or more than about 50%, 60%, 75%, 80%, 85%, 90%, 95%, 97.5%, 99%, or more. Optimal alignment may be determined with the use of any suitable algorithm for aligning sequences, non-limiting example of which include the Smith-Waterman algorithm, the Needleman-Wunsch algorithm, algorithms based on the Burrows-Wheeler Transform (e.g. the Burrows Wheeler Aligner), ClustalW, Clustal X, BLAT, Novoalign (Novocraft Technologies, ELAND (Illumina, San Diego, Calif.), SOAP (available at soap.genomics.org.cn), and Maq (available at maq.sourceforge.net). In some embodiments, a guide sequence is about or more than about 5, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 35, 40, 45, 50, 75, or more nucleotides in length. In some embodiments, a guide sequence is less than about 75, 50, 45, 40, 35, 30, 25, 20, 15, 12, or fewer nucleotides in length.

III. ISOLATED RECOMBINANT CELLS

Aspects of the presently disclosed subject matter relate to an isolated recombinant cell comprising an expression vector of the presently disclosed subject matter. In some embodiments, host cells which contain the constructs and vectors of the presently disclosed subject matter are also encompassed, e.g. in vitro cells such as cultured cells, e.g., bacterial or eukaryotic cells which are used to store generate or manipulate the vectors, and the like. In some embodiments, the isolated recombinant cell or host cell is a mammalian cell. In some embodiments, the isolated recombinant cell or host cell is a human cell. In some embodiments, the cell is selected from the group consisting of a bacterial cell and a eukaryotic cell. In some embodiments, the eukaryotic cell is a mammalian cell. In some embodiments, the eukaryotic cell is a human cell.

IV. KITS

Aspects of the presently disclosed subject matter relate to kits for modulating the expression levels of polypeptides in cells. In general, a presently disclosed kit contains some or all of the components, reagents, supplies, and the like to practice a method according to the presently disclosed subject matter.

In some embodiments, the term “kit” may refer to any intended article of manufacture (e.g., a package or a container) comprising at least one of the presently disclosed engineered nuclease, expression vector, isolated recombinant cell comprising the expression vector, and instructions for modulating expression of an endogenous polypeptide using an engineered nuclease or recombinant polypeptide of interest using the expression vector and/or the isolated recombinant cell. The kit can be packaged in a divided or undivided container, such as a carton, bottle, ampule, tube, etc. The presently disclosed compositions can be packaged in dried, lyophilized, or liquid form. Additional components provided can include vehicles for reconstitution of dried components. Preferably all such vehicles are sterile and apyrogenic so that they are suitable for injection into a patient without causing adverse reactions.

The polynucleotide sequences for use in the methods, expression vectors, and kits of the presently disclosed subject matter may encode one or more bioactive molecules functional in the treatment of a disease, disorder, or condition. The one or more bioactive molecules may be selected from the group consisting of proteins, polypeptides, peptides, drugs, enzymes, and hormones.

In some embodiments, the kit can be used for highthrougput purification and quantification of a recombinant polypeptide of interest to be expressed. The kit may include a presently disclosed expression vector for expressing a recombinant polypeptide of interest in a host cell. In some embodiments, the kit includes an affinity chromatography resin, a proteolytic enzyme, an internal quantification standard, a matrix for MALDI-TOF mass spectrometry, and instructions for use. In some embodiments, the kit includes at least one buffer selected from the group consisting of a lysis buffer, a denaturing buffer, an affinity chromatography binding buffer, an affinity chromatography washing buffer, an affinity chromatography elution buffer, and a proteolytic digestion buffer. In some embodiments, the kit for high throughput purification and quantification includes at least one multi-well plate. In some embodiments, the kit for high throughput purification and quantification includes a partially or fully automated high throughput purification and quantification system.

V. METHODS OF PRODUCING POLYPEPTIDES

Aspects of the presently disclosed subject matter relate to methods of producing a polypeptide of interest (e.g., a recombinant polypeptide) that involve culturing a recombinant cell of the presently disclosed subject matter in vitro under conditions suitable for the tunable expression of the polypeptide of interest in the cell. In some embodiments, the method optionally includes recovering the polypeptide of interest. In some embodiments, a kit of the presently disclosed subject matter can be used to produce a polypeptide of interest.

VI. RECOMBINANT POLYPEPTIDES

Aspects of the presently disclosed subject matter relate to recombinant polypeptides produced according to a method of the presently disclosed subject matter. In some aspects, a recombinant polypeptide of interest can be produced using an expression vector of the presently disclosed subject matter. In other aspects, a recombinant polypeptide of interest can be produced in an isolated recombinant cell of the presently disclosed subject matter. In certain easpects, a recombinant polypeptide of interest can be produced using a kit of the presently disclosed subject matter. As used herein, “polypeptide of interest” refers to any polypeptide for which the tunable regulation of its expression is desired in cells. In some embodiments, the polypeptide of interest comprises a therapeutic antibody, peptide, protein, or enzyme. In some embodiments, the polypeptide of interest comprises a naturally occurring polypeptide. In some embodiments, the polypeptide of interest comprises a variant of a naturally occurring polypeptide. In some embodiments, the polypeptide of interest comprises a fusion protein. In some embodiments, the polypeptide of interest comprises a label or tag. In some embodimenst, the polypeptide of interest comprises a reporter. In some embodiments, the polypeptide of interest comprises at least one N-terminus HA tag and/or at least one C-terminus reporter, such as a fluorescent protein. In some embodiments, the polypeptide of interest is a naturally occurring mammalian protein or a variant thereof. In some embodiments, the polypeptide of interest comprises a human protein or a variant thereof. In some embodiments, the polypeptide of interest comprises a C-terminus polylysine track or tag (e.g., a polyA polynucleotide sequence tag, a polyAAG lysine polynucleotide sequenc tag, etc.). In some embodiments, the polypeptide of interest comprises a N-terminus polylysine track or tag (e.g., a polyA polynucleotide sequence tag, a polyAAG lysine polynucleotide sequenc tag, etc.).

VII. GENERAL DEFINITIONS

Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation. Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this presently described subject matter belongs.

Following long-standing patent law convention, the terms “a,” “an,” and “the” refer to “one or more” when used in this application, including the claims. Thus, for example, reference to “a subject” includes a plurality of subjects, unless the context clearly is to the contrary (e.g., a plurality of subjects), and so forth.

Throughout this specification and the claims, the terms “comprise,” “comprises,” and “comprising” are used in a non-exclusive sense, except where the context requires otherwise. Likewise, the term “include” and its grammatical variants are intended to be non-limiting, such that recitation of items in a list is not to the exclusion of other like items that can be substituted or added to the listed items.

For the purposes of this specification and appended claims, unless otherwise indicated, all numbers expressing amounts, sizes, dimensions, proportions, shapes, formulations, parameters, percentages, parameters, quantities, characteristics, and other numerical values used in the specification and claims, are to be understood as being modified in all instances by the term “about” even though the term “about” may not expressly appear with the value, amount or range. Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are not and need not be exact, but may be approximate and/or larger or smaller as desired, reflecting tolerances, conversion factors, rounding off, measurement error and the like, and other factors known to those of skill in the art depending on the desired properties sought to be obtained by the presently disclosed subject matter. For example, the term “about,” when referring to a value can be meant to encompass variations of, in some embodiments, ±100% in some embodiments ±50%, in some embodiments ±20%, in some embodiments ±10%, in some embodiments ±5%, in some embodiments ±1%, in some embodiments ±0.5%, and in some embodiments ±0.1% from the specified amount, as such variations are appropriate to perform the disclosed methods or employ the disclosed compositions.

Further, the term “about” when used in connection with one or more numbers or numerical ranges, should be understood to refer to all such numbers, including all numbers in a range and modifies that range by extending the boundaries above and below the numerical values set forth. The recitation of numerical ranges by endpoints includes all numbers, e.g., whole integers, including fractions thereof, subsumed within that range (for example, the recitation of 1 to 5 includes 1, 2, 3, 4, and 5, as well as fractions thereof, e.g., 1.5, 2.25, 3.75, 4.1, and the like) and any range within that range.

EXAMPLES

The following examples are included to demonstrate various embodiments of the present disclosure. It should be appreciated by those of skill in the art that the techniques disclosed in the examples that follow represent techniques discovered by the inventors to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

EXAMPLE 1: In Translational Regulation, Poly(A) Coding Sequences in Human Cells Unexpectedly Induce Ribosome Pausing Directly, without a Role for the Encoded Basic Peptide

Bioinformatic analysis can be used as an initial approach to ask whether there are evolutionary constraints that limit the abundance of polybasic amino acid residues. Runs of polybasic residues in coding sequences of genes from many eukaryotic organisms are under-represented when compared to runs of other amino acids (Karlin et al. (2002) Proc. Natl. Acad. Sci. U.S.A 99, 333-338). Interestingly, polyarginine runs have a similar abundance to polylysine runs at each segment length across multiple organisms (FIG. 1A, FIG. 1B). A series of mCherry reporters were developed to evaluate the effects of polybasic sequences on translation efficiency (output). The reporter construct consists of a double HA-tag, a run of control or polybasic sequences, followed by the mCherry reporter sequence (HAmCherry, FIG. 2A). As a control for DNA transfection and in vivo fluorescence measurements, a construct with green fluorescent protein (GFP) was also created. The reporters were used to ask whether the polybasic sequences influence translation of reporter sequences in neonatal human fibroblasts (HDFs) as well as in Drosophila S2 cells and Chinese hamster ovary cells (CHO) (FIG. 2B, FIG. 2C, FIG. 3A, FIG. 3B, FIG. 4A, FIG. 4B). Expression of the mCherry reporter was followed using fluorescence at 610 nm in vivo or western blot analyses of samples collected 48 hours after transfection (FIG. 2B, FIG. 2C). The stability of reporter mRNAs was determined using standard quantitative reverse transcription polymerase chain reaction assay (qRT-PCR, (Djuranovic et al. (2012) Science. 336, 237-240) (FIG. 2D). By careful primer design, this method allows estimation of the level of endonucleolytic cleavage on mRNAs with stalled ribosome complexes.

The results of DNA transfections indicate that strings of lysine codons specifically inhibit translation and decrease the stability of the mCherry reporter mRNA while up to 12 arginine codons (AGG and CGA) have much less, if any effect, on either translation or mRNA stability (FIG. 2B, FIG. 2C, FIG. 2D, FIG. 3A, FIG. 3B, FIG. 4A, FIG. 4B). The potency of translational repression by lysine codons is clearly seen with as few as six AAA-coded lysines (AAA6) and increases with the length of the homo-polymeric amino acid run. It is also noted that the levels of expressed mCherry reporters (FIG. 2B, FIG. 2C) correlate with the stability of their mRNAs (FIG. 2D), consistent with earlier published observations (Doma and Parker (2006) Nature 440, 561-564; Dimitrova et al. (2009) J. Biol. Chem. 284,10343-10352; Tsuboi et al. (2012) Mol. Cell. 46, 518-529). To control for possible transcriptional artifacts due to the effects of homopolymeric sequence on transcription by RNA polymerase, mRNAs synthesized in vitro by T7 RNA polymerase were electroporated directly into HDF cells. Previous studies established that T7 RNA polymerase is able to transcribe such homopolymeric sequences with high fidelity (Koutmou et al. (2015) eLIFE 10.7554/eLife.05534; Djuranovic et al. (2012) Science. 336, 237-240). Results of the mRNA electroporation work reproduced DNA transfection experiments, consistent with models of translational repression triggered by lysine codons (FIG. 5A, FIG. 5B). To assess whether the stability of polylysine reporter mRNAs is dependent on translation, the translation initiation inhibitor harringtonine (Fresno et al. (1977) Eur. J. Biochem. FEBS. 72, 323-330) was introduced into HDF cells prior to mRNA electroporation. In this case, a significant change in mRNA stability between wild type and polylysine-encoding mCherry constructs was not observed (FIG. 6A, FIG. 6B, FIG. 6C); these data indicate that accelerated decay of polylysine mCherry mRNAs is dependent on translation. Consistent with this observation, the insertion of 36As (sequence equivalent to twelve lysine AAA codons) after the stop codon, in the 3′UTR region, did not affect the protein expression level or mRNA stability of the assayed construct (FIG. 7A, FIG. 7B, FIG. 7C). Insertion of polylysine codons at different positions along the coding sequence drastically reduced reporter expression and mRNA levels independent of the relative position in the construct. As such, it follows that the observed changes in mRNA stability (FIG. 2D) result from translation-dependent processes.

The most striking observation from these data is that the production of polylysine constructs is codon dependent; runs of polylysine residues coded by AAA codons have a much larger effect on the protein output from reporter constructs than an equivalent run of lysine AAG codons (FIG. 2B, FIG. 2C, FIG. 2D, FIG. 3A, FIG. 3B, FIG. 4A, FIG. 4B, FIG. 5A, FIG. 5B, FIG. 6A, FIG. 6B, FIG. 6C, FIG. 7A, FIG. 7B, FIG. 7C, FIG. 8A, FIG. 8B, FIG. 8C). This effect is unlikely to be driven by the intron-less nature of the reporter since constructs containing human hemoglobin gene (delta chain, HBD) with two introns showed the same effect on protein output and RNA stability (FIG. 8A, FIG. 8B, FIG. 8C). It is also noted that this effect is unlikely to be driven simply due to tRNALys abundance, since the relative protein expression and mRNA stability are comparable in cells from various species that do not share similar tRNA abundance profiles (gtrnadb.ucsc.edu/; FIG. 2A, FIG. 2B, FIG. 2C, FIG. 2D, FIG. 3A, FIG. 3B, FIG. 4A, FIG. 4B, FIG. 5A, FIG. 5B, FIG. 6A, FIG. 6B, FIG. 6C, FIG. 7A, FIG. 7B, FIG. 7C, FIG. 8A, FIG. 8B, FIG. 8C). Furthermore, the human genome encodes a comparable number of tRNA genes for AAA and AAG codons (gtrnadb.ucsc.edu/Hsapi19/) and general codon usage is similar (0.44 vs 0.56, AAA vs AAG). The generality of codon-dependent polylysine protein production was recently documented in E. coli cells where a single tRNALys(UUU) decodes both AAA and AAG codons (Koutmou et al. (2015) eLIFE 10.7554/eLife.05534).

In light of these experimental observations, codon usage and the distribution of lysine codons in polylysine tracks in various species was systematically explored (FIG. 9 ). Remarkably, a strong under-representation of poly(A) nucleotide runs in regions coding for iterated lysines (even with as few as three lysines) in human genes is found (FIG. 9 ). When there are four iterated lysine residues, the difference between expected (from data for all lysine residues) and observed codon usage for four AAA codons in a row is over one order of magnitude (FIG. 10 ). Notably, similar patterns of codon usage in lysine poly(A) tracks are observed in other vertebrates (FIG. 11 ).

Ribosome profiling data have the potential to reveal features of pausing on polybasic stretches throughout the genome (Ingolia (2014) Nat. Rev. Gen. 15, 205-213). A cumulative analysis of three ribosome profiling datasets from human cells for regions encoding four lysines in a row revealed that the occupancy pattern on four lysines encoded by three AAA and one AAG codon is different from the pattern for two, three and four AAG codons in four lysine-tracks (FIG. 12A). The latter three resemble the occupancy pattern for tracks of arginines (FIG. 13A, FIG. 13B), which is similar to the ribosome stalling on runs of basic amino acids observed by other researchers (Charneski and Hurst (2013) PLoS Biol. 11, e1001508). This suggests that the observed effect on protein output and mRNA stability is dependent on nucleotide, not simply the amino acid sequence. Additionally, the first example (with three AAA and one AAG codon) has a region of increased ribosome occupancy found additionally after the analyzed region (FIG. 12A). Together, these data suggest that attenuation of translation on poly(A) nucleotide tracks occurs via a different mechanism than just the interaction of positively charged residues with the negatively charged ribosomal exit tunnel.

In order to probe the potential impact of the observed disparities in codon distribution for runs of three and four consecutive lysine codons, runs of three lysine resides with various numbers of consecutive As (A9-A13) were inserted into the mCherry reporter construct (FIG. 12B). As in the previous experiments (FIG. 2B, FIG. 2C), the expression of the mCherry reporter as well as the stability of the mRNA was followed (FIG. 12C, FIG. 12D, FIG. 12E). It was found that the insertion of sequences with 12 or more consecutive As reduces mCherry reporter expression by more than 50% with comparable effects on mRNA stability. Importantly, in each construct, no more than three lysines are encoded so the increasing effect on protein output must result from consecutive As, not Ks.

Next, it was asked whether polylysine sequences from naturally occurring genes have the same general effect on expression of reporter protein. To take an unbiased approach, different lengths of homopolymeric lysine runs and various distributions of AAA and AAG codons were selected (FIG. 14A). Reporter constructs with lysine runs were electroporated into HDF cells and relative amounts of reporter expression and mRNA stability were evaluated (FIG. 14B, FIG. 14C). As with the designed sequences in FIG. 12B, the observed decreases in reporter protein expression and mRNA stability correlated with the number of consecutive A nucleotides and not with total number of lysine codons in the chosen sequences. The reporter experiments together (FIG. 2B, FIG. 2C, FIG. 2D, FIG. 3A, FIG. 3B, FIG. 4A, FIG. 4B, FIG. 5A, FIG. 5B, FIG. 6A, FIG. 6B, FIG. 6C, FIG. 7A, FIG. 7B, FIG. 7C, FIG. 8A, FIG. 8B, FIG. 8C, FIG. 12B, FIG. 12C, FIG. 12D, FIG. 12E, FIG. 14A, FIG. 14B, FIG. 14C) argue that the repressive effects of the polylysine sequence are caused by iterated poly(A) tracks rather than by runs of encoded lysine residues. Similar effects were recently documented in in vivo and in vitro experiments with E. coli cells or a purified translational system, respectively (Koutmou et al. (2015) eLIFE 10.7554/eLife.05534). The differences observed in expression of reporter sequences with poly(A) nucleotide tracks from human genes favor the possibility that such regions in natural genes play a “translational attenuator” role that can modulate overall protein expression.

TABLE 1 shows a table of overrepresentation of gene ontology terms for 456 genes containing polyA tracks in heir coding regions up to P-value of 0.05 Term Background frequency Sample frequency Expected +/− P-value nucleic acid binding 3799 149 7.614e+01 + 60651e−15  (GO:003676) heterocyclic compound binding 5648 189 1.132e+02 + 5.339e−13 (GO:1901363) RNA binding 1500 79 3.006e+01 + 7.430e−13 (GO:003723) organinc cyclic compound binding 5717 190 1.146e+02 + 8.553e−13 (GO:097159) poly(A) RNA binding 1122 62 2.249e+01 + 1.388e−10 (GO:044822) binding 12444 316 2.494e+02 + 5.325e−09 (G0:0005488) DNA binding 2322 87 4.654e+01 + 1.491e−06 (GO:003677) protein binding 8307 219 1.665e+02 + 3.725e−05 (GO:005515) ion binding 5844 166 1.171e+02 + 3.815e−05 (GO:043167) chromatin binding 409 26 8.197e+00 + 6.569e−05 (GO:003682) zinc ion binding 1181 49 2.367e+01 + 2.713e−04 (GO:008270) molecular_function 15480 353 3.103e+02 + 3.165e−04 (GO:003674) transition metal ion binding 1417 52 2.840e+01 + 3.844e−03 (GO:046914) ATP binding 1430 52 2.886e+01 + 4.880e−03 (GO:005524) nucleotide binding 2264 73 4.538e+01 + 6.077e−03 (GO:000166) nucleoside phosphate binding 2265 73 4.540e+01 + 6.164e−03 (GO:1901265) adenyl ribonucleotide binding 1465 52 2.936e+01 + 9.081e−03 (GO:032559) adenyl nucleotide binding 1483 52 2.972e+01 + 1.235e−02 (GO:030554) protein serine/threonine kinase activity 434 22 8.698e+00 + 1.523e−02 (GO:004674) nucleoside-triphosphate activity 707 30 1.417e+01 + 2.103e−02 (GO:017111) purine ribonucleotide triphosphate binding 1760 58 3.527e+01 + 2.439e−02 (GO:035639) purine ribonucleotide binding 1801 59 3.610e+01 + 2.486e−02 (GO:032555) purine ribonucleoside binding 1769 58 3.545e+01 + 2.783e−02 (GO:032550) purine nucleoside binding 1772 58 3.551e+01 + 2.908e−02 (GO:001883) ribonucleoside binding 1773 58 3.553e+01 + 2.950e−02 (GO:032549) ribonucleotide binding 1816 59 3.640e+01 + 3.087e−02 (GO:032553) purine nucleotide binding 1821 59 3.650e+01 + 3.315e−02 (GO:017676) nucleoside binding 1785 58 3.574e+01 + 3.409e−02 (GO:001882) protein kinase activity 591 26 1.184e+01 + 3.421e−02 (GO:004672) helicase activity 145 11 2.906+00 + 3.556e−02 (GO:004386) small molecule binding 2539 76 5.089e+01 + 4.353e−02 (GO:036094)

Based on the results with insertion of 12 consecutive A nucleotides (FIG. 12C) and endogenous A-rich sequences (FIG. 14B), it is proposed that a run of 11As in a stretch of 12 nucleotides (12A-1 pattern) will typically yield a measurable effect on protein expression. Since the A string did not require beginning in any particular codon frame, the sequence may not necessarily encode four consecutive lysines. As such, the 12A-1 pattern has been used to search the cDNA sequence database for multiple organisms (NCBI RefSeq resource; Pruitt et al. (2014) Nucleic Acids Res. 42, D756-763). This query revealed over 1800 mRNA sequences from over 450 human genes; the proportion was similar in other vertebrates (Table 5). Gene ontology analyses revealed an over-representation of nucleic acid binding proteins, especially RNA binding and poly(A) RNA binding proteins (Table 1). The positions of poly(A) tracks are distributed uniformly along these identified sequences with no significant enrichment towards either end of the coding region (FIG. 14D). The proteins encoded by these mRNAs are often conserved among eukaryotes; of the 7636 protein isoforms coded by mRNA with poly(A) tracks from human, mouse, rat, cow, frog, zebrafish and fruit fly, 3877 are classified as orthologous between at least two organisms. These orthologous proteins share very similar codon usage in the poly-lysine track, as seen in the example of the RASAL2 tumor suppressor protein (McLaughlin et al. (2013) Cancer Cell. 24, 365-378) (FIG. 15 ). These observations are consistent with the idea that poly(A) tracks may regulate specific sets of genes in these different organisms. Additional analyses of the ribosome profiling data for mRNAs from selected pools of genes (12A-1 pattern genes) showed an increased number of ribosome footprints (RPFs) in sequences following the poly(A) tracks (FIG. 13A, FIG. 13B). The observed pattern was similar, albeit more pronounced, to the pattern observed for four lysine tracks encoded by three AAA codons and one AAG (FIG. 2A), despite the fact that in many cases the selected pattern did not encode four lysines.

Given the strong sequence conservation and possible role in modulation of protein expression, the effects of mutations in poly(A) tracks were further explored. The reporter constructs containing poly(A) nucleotide tracks from endogenous genes (ZCRB1, MTDH and RASAL2) were used to evaluate effects of synonymous lysine mutations in these poly(A) tracks on protein expression (FIG. 16A, FIG. 16B, FIG. 16C, FIG. 17A, FIG. 17B, FIG. 17C, FIG. 18A, FIG. 18B, FIG. 18C). In each construct, mutations were made that changed selected AAG codons to AAA, increasing the length of consecutive As. Alternatively, AAA to AAG changes were introduced to create interruptions in poly(A) tracks. Reporter constructs with single AAG-to-AAA changes demonstrate consistent decreases in protein expression and mRNA stability. Conversely, AAA-to-AAG changes result in increases in protein expression and mRNA stability (FIG. 16B, FIG. 16C, FIG. 17A, FIG. 17B, FIG. 17C, FIG. 18A, FIG. 18B, FIG. 18C).

It was next asked whether the same synonymous mutations have similar effects when cloned in the full-length coding sequence of the ZCRB1 gene (FIG. 16D, FIG. 16E, FIG. 16F, FIG. 19A, FIG. 19B, FIG. 19C, FIG. 19D). Indeed, the effects on protein and mRNA levels observed with the mCherry reporter sequences are reproduced within the context of the complete coding sequence of the ZCRB1 gene (and mutated variant). Mutation of single AAG-to-AAA codons in the poly(A) track of the ZCRB1 gene (K137K; 411G>A) resulted in a significant decrease in both protein expression and mRNA stability (FIG. 16E, FIG. 16F, FIG. 19A, FIG. 19B, FIG. 19C, FIG. 19D); substitution of two AAA codons with synonymous AAG codons (K136K:408 A>G; K139K:417A>G) resulted in increases in both recombinant ZCRB1 protein output and mRNA stability. Generally, mutations resulting in longer poly(A) tracks reduced protein expression and mRNA stability, while synonymous substitutions that result in shorter poly(A) nucleotide tracks increased both protein expression and mRNA stability. From these observations, it is suggested that synonymous mutations in poly(A) tracks could modulate protein production from these genes.

Poly(A) tracks resemble ribosome “slippery” sequences that have been associated with translational frame-shifts (Belfield et al. (2007) Nucleic Acids Res. 35, 1322-1332; Chen et al. (2014) Nature 512, 328-332). Recent studies suggest that polyA tracks can induce “sliding” of E. coli ribosomes resulting in frameshifting (Koutmou et al. (2015) eLIFE 10.7554/eLife.05534; Yan et al. (2015) Cell 160(5), 870-81). Therefore, potential frame-shifted products of overexpressed ZCRB1 variants were looked for by immuno-precipitation using an engineered N-terminally located HA-tag. It was observed that the presence of a protein product of the expected size results from possible frame-shifting in the construct with increased length A tracts (ZCRB K137K (411G>A) mutant) (FIG. 21A). The presence of potential frame-shifted protein products was not observed in WT or control double synonymous mutations K136K(408 A>G):K139K(417A>G). Interestingly, it was noted that the K137K-synonymous change represents a recurrent cancer mutation found in the COSMIC database (COSMIC stands for Catalogue of Somatic Mutations in Cancer, cancer.sanger.ac.uk; Forbes et al. (2014) Nucleic Acids Res.) for ZCRB1 gene; cancersangerac.uk/cosmic/mutation/overview?id=109189). Similar results were obtained when immuno-precipitations were compared of overexpressed and HA-tagged wild type MTDH gene and a K451 K (1353 G>A) variant, yet another cancer-associated mutation (cancer.sanger.ac.uk/cosmic/mutation/overview?id=150510; FIG. 22A, FIG. 22B).

To further document the extent and direction of frame-shifting in the ZCRB1 transcript, polyA tracks were introduced from WT ZCRB1 and a K137K ZCRB1 mutant into a Renilla luciferase reporter gene. Single or double nucleotide(s) were introduced downstream in the reporter sequence following the A track, thus creating +1 and −1 frame-shift (FS) constructs, respectively (FIG. 20B). When compared to wild type ZCRB1 polyA track, the G>A mutant shows decreases in full length luciferase protein expression (approximately 40% reduction in “zero” frame); additionally, the G>A mutant exhibits an increase in expression of −1 FS frame construct (which is not observed in the wild type ZCRB1 poly(A) track −1 FS construct) (FIG. 20C). The total amount of luciferase protein activity from the −1 FS ZCRB1 G>A mutant construct is approximately 10% of that expressed from the “zero” frame mutant construct (FIG. 20C, FIG. 22A, FIG. 22B). No significant change in luciferase expression was detected in samples electroporated with +1 FS constructs where expression from these constructs resulted in background levels of luciferase activity (FIG. 21A, FIG. 21B).

Frame-shifting and recognition of out-of-frame premature stop codons can lead to nonsense-mediated mRNA decay (NMD) that results in targeted mRNA decay (Belew et al. (2011) Nucleic Acids Res. 39, 2799-2808; Belew et al. (2014) Nature. 512, 265-269). Previous efforts suggest that NMD may play a role in determining the stability of poly(A) track-containing mRNAs. Deletion of NMD factor Upf1p in yeast cells partially rescues mRNA levels from constructs with simple poly(A) tracks (Koutmou et al. (2015) eLIFE 10.7554/eLife.05534). The complete set of human poly(A) track-containing genes have been analyzed to see whether they would be likely targets for NMD as a result of frameshifting on the poly(A) track (based on the usual rules for NMD; Lykke-Andersen et al. (2000) Cell. 103,1121-1131; Le Hir et al. (2001) EMBO J. 20, 4987-4997; Chang et al. (2007) Annu. Rev. Biochem. 76, 51-74; Popp and Maquat (2013) Annu. Rev. Genet. 47, 139-165). Based on the position of the poly(A) tracks, and their position relative to possible PTCs in the −1 and +1 frame, and the location of downstream exon-intron boundaries, a part of the genes of interest would likely be targeted by NMD as a result of frame-shifting during poly(A)-mediated stalling (these transcripts and position of PTCs are listed in Table 2). The considerable number of human poly(A) track genes may not elicit NMD response since PTCs in both −1 and +1 frame following poly(A) tracks are less than 50 nucleotides away from established exon-intron boundaries. While the majority of frame-shift events seem to lead to proteins that would be truncated immediately after poly(A) tracks, in a few cases a novel peptide chain of substantial length may be produced (Table 3). As such, the outcome of poly(A) track stalling and slipping may include a scenario in which a frame-shifted protein product is synthesized in addition to the full-length gene product (scheme shown in FIG. 20D). The possible role and presence of such fragments from poly(A) track genes and their variants is still to be elucidated.

TABLE 2 shows a table of mRNAs that have intron-exon boundary closer than 50 nucleotides downstream from a stop codon arising from frameshifting over polyA tracks. These genes would fall in the category of non “classical” NMD targets if frameshifting occurs on polyA track. location of location of end of nearest location of downstream end of downstream mRNA GI polyA stop stop intron-exon mRNA GI polyA nearest stop intron-exon number region codon codon boundary number region codon boundary 315360663 465 TAG 472 491 239787843 177 TAG 321 315360663 465 TGA 467 491 217035143 1437 TAG 1467 54792083 710 TAG 839 849 188035876 1539 TAA 1553 61743937 294 TAA 310 327 188035876 1539 TGA 1545 61743937 294 TAG 324 327 312283645 1473 TAA 1503 61743937 294 TGA 306 327 291084574 1802 TAG 2242 41350197 346 TGA 385 398 291084574 1802 TGA 1832 42542385 1274 TAA 1312 1342 312434029 1760 TAA 1790 115430109 97 TAA 139 171 21536424 476 TAA 508 115430109 97 TAG 321 340 21536424 476 TGA 515 115430109 97 TGA 162 171 312283632 1760 TAA 1790 38327633 431 TGA 452 470 393185915 487 TAG 498 148596997 396 TGA 411 416 393185915 487 TGA 523 146133847 192 TAA 473 499 187761329 1522 TGA 1553 146133847 192 TAG 200 246 557786140 263 TAA 265 189163500 2545 TAG 2788 2813 296278211 1102 TAA 1184 214010231 475 TAA 748 780 296278220 493 TAA 575 284795238 986 TAG 997 1014 257467646 2736 TGA 2785 284795238 986 TGA 1001 1014 385648269 3155 TAA 3253 332205944 3430 TAA 3688 3732 385648269 3155 TAG 3260 283549152 927 TGA 996 1015 27894332 928 TAG 1071 325197190 472 TAA 484 515 27894332 928 TGA 942 325197190 472 TGA 502 515 350606366 375 TAA 464 325197194 1713 TAA 1725 1756 350606366 375 TAG 434 325197194 1713 TGA 1743 1756 317008579 4447 TGA 4458 325197181 768 TAA 780 811 209915559 770 TAG 825 325197181 768 TGA 798 811 296278213 618 TAA 700 332205942 3451 TAA 3709 3753 350606370 621 TAA 710 378786661 207 TAA 304 352 350606370 621 TAG 680 378786661 207 TAG 351 352 350606369 438 TAG 497 378786661 207 TGA 364 408 385648267 3393 TAA 3491 367460089 3008 TAA 3256 3288 385648267 3393 TAG 3498 378786660 315 TAA 412 460 61744441 448 TGA 466 378786660 315 TAG 459 460 312283650 1601 TAA 1631 378786660 315 TGA 472 516 589811545 2995 TGA 3044 387528005 1266 TAG 1416 1437 387527983 928 TGA 942 57863258 885 TAG 938 947 197245388 940 TAA 1013 380420368 574 TAG 821 842 197245388 940 TGA 968 527317397 1917 TGA 1941 1958 262399360 1971 TAG 2015 543173130 2544 TAG 2847 2872 262399359 1962 TAG 2006 347954818 953 TGA 1010 1038 283806678 8679 TAG 8790 564473350 2511 TAA 2513 2521 189242611 609 TAG 944 585420399 1248 TAG 1381 1407 365812503 1512 TAG 1515 585420411 916 TAG 1049 1075 365812503 1512 TGA 1522 256542287 192 TAA 473 499 153792693 6916 TAG 6952 256542287 192 TAG 200 246 70980548 254 TAG 312 223634474 186 TAA 467 493 38683845 918 TAA 924 223634474 186 TAG 194 240 38683845 918 TAG 959 585866348 1248 TAG 1381 1407 38683845 918 TGA 981 110349755 889 TGA 926 951 148612837 2289 TAG 2586 110349753 889 TGA 926 951 47419908 2793 TAA 2807 544583528 866 TAA 980 1012 47419908 2793 TAG 2821 93277100 828 TAA 855 903 47419908 2793 TGA 2795 145699132 2771 TAA 2772 2777 21361597 1222 TGA 1225 93141224 645 TAG 649 667 291190786 1506 TAG 1514 527317380 612 TAA 693 696 67944632 259 TAG 391 32967604 1594 TAG 1683 1697 67944631 259 TAG 391 72377390 216 TAG 281 318 67944633 415 TAG 547 153251835 867 TAA 901 905 122114650 3206 TAA 3430 153251835 867 TGA 872 905 109715821 865 TAA 991 215272324 361 TGA 421 464 109715821 865 TAG 1082 46255020 219 TGA 226 247 109715821 865 TGA 917 116063563 3480 TAA 3534 3538 154354989 1512 TAG 1515 116063563 3480 TGA 3509 3538 154354989 1512 TGA 1522 194473999 931 TAA 998 1004 47419910 2895 TAA 2909 56550119 511 TAA 525 559 47419910 2895 TAG 2923 56550119 511 TAG 531 559 47419910 2895 TGA 2897 564473377 1659 TAA 1661 1669 216548486 1594 TGA 1632 151301227 2638 TAA 2698 2723 189491764 1859 TGA 1943 451172080 719 TAG 775 808 189242610 609 TAG 944 451172080 719 TGA 770 808 315360659 761 TAG 768 94538358 192 TAA 473 499 315360659 761 TGA 763 94538358 192 TAG 200 246 114155141 2355 TAA 2463 119637838 1257 TAG 1275 1304 114155141 2355 TAG 2450 119637838 1257 TGA 1288 1304 75677575 956 TAA 959 49640008 6092 TAA 6105 6154 75677575 956 TAG 971 49640008 6092 TGA 6114 6154 325197180 604 TAA 616 49640010 4801 TAA 4814 4863 325197180 604 TGA 634 49640010 4801 TGA 4823 4863 189409141 1081 TAA 1134 239787903 1353 TAA 1428 1472 189409141 1081 TAG 1156 239787903 1353 TAG 1469 1472 91208427 6031 TAA 6289 239787903 1353 TGA 1442 1472 115527086 2080 TGA 2087 55749880 458 TGA 519 549 125656164 2810 TAG 2926 225579091 2672 TAA 2683 2705 61635914 967 TGA 974 225579091 2672 TGA 2695 2705 183227692 581 TAA 618 125987600 747 TAA 858 889 183227692 581 TGA 625 187828563 1100 TAA 1112 1153 51873042 1122 TAG 1187 451172082 569 TGA 733 764 189163502 2545 TAG 2788 451172084 533 TAG 589 622 148746212 2045 TAG 2114 451172084 533 TGA 584 622 148746212 2045 TGA 2099 451172086 533 TGA 697 728 122937397 8679 TAG 8790 270483794 1195 TGA 1196 1203 284795235 1103 TAG 1114 209870068 878 TAA 940 985 284795235 1103 TGA 1118 72377376 305 TAG 370 407 392307008 2145 TAA 2393 63054847 785 TGA 789 820 124107605 853 TAA 861 573459699 766 TAA 781 801 124107605 853 TGA 864 573459699 766 TGA 893 915 385648266 3527 TAA 3625 116642876 1399 TAG 1450 1493 385648266 3527 TAG 3632 116642876 1399 TGA 1457 1493 325053711 956 TAA 959 188219548 1077 TAA 1084 1113 325053711 956 TAG 971 188219548 1077 TAG 1103 1113 325053712 956 TAA 959 544583488 906 TAA 1020 1052 325053712 956 TAG 971 543173126 2619 TAG 2922 2947 392307006 2628 TAA 2876 544346128 1063 TAG 1145 1189 459215048 2072 TAG 2147 544346128 1063 TGA 1232 1257 388490157 3286 TGA 3323 170650704 667 TAA 807 830 32483358 2382 TAA 2485 170650704 667 TAG 798 830 32483358 2382 TGA 2449 544583450 918 TAA 1032 1064 291290967 5965 TAG 6092 289547540 894 TAA 992 1033 291084578 1907 TAG 2347 367460086 2981 TAA 3229 3261 291084578 1907 TGA 1937 51243064 631 TGA 638 656 307746920 769 TAG 802 215599550 501 TAG 662 689 32483365 2349 TAA 2452 475505353 3017 TAA 3256 3290 32483365 2349 TGA 2416 122937226 703 TAA 731 738 531990837 1144 TAA 1153 122937226 703 TAG 855 869 531990837 1144 TGA 1184 122937395 987 TAA 1025 1028 32483360 2382 TAA 2485 122937395 987 TAG 1032 1072 32483360 2382 TGA 2449 122937395 987 TGA 1020 1028 22027649 707 TAG 787 57863256 971 TAG 1024 1033 22027649 707 TGA 782 451172081 569 TAG 625 658 350606365 491 TAA 580 451172081 569 TGA 620 658 350606365 491 TAG 550 87298936 1370 TAA 1453 1487 459215047 2072 TAG 2147 138175816 1579 TAA 1583 1610 291575138 897 TAG 1023 138175816 1579 TGA 1580 1610 531990838 858 TAA 868 150036261 475 TAA 575 602 531990838 858 TGA 899 150036261 475 TGA 476 493 353411933 747 TAG 751 315360661 566 TAG 573 592 313661425 3742 TGA 3757 315360661 566 TGA 568 592 257467647 3543 TGA 3592 38373672 3210 TAG 3474 3489 388490159 3786 TGA 3823 38373672 3210 TGA 3244 3290 531990840 822 TAA 832 544346132 1174 TAG 1256 1300 531990840 822 TGA 863 544346132 1174 TGA 1343 1368 354682004 903 TAG 1487 116805347 219 TGA 261 278 354682006 1473 TAA 1583 157502183 1552 TAA 1882 1906 354682006 1473 TAG 1484 23111022 714 TAG 721 740 354682006 1473 TGA 1572 23111022 714 TGA 716 740 32483364 2349 TAA 2452 32967602 1594 TAG 1683 1697 32483364 2349 TGA 2416 573459727 352 TAA 367 387 305410828 910 TAG 942 573459727 352 TGA 479 501 467091961 1974 TAA 1981 573459714 617 TAA 632 652 467091961 1974 TAG 2146 573459714 617 TGA 744 766 467091961 1974 TGA 1990 574275032 622 TGA 629 633 401664559 8145 TAG 8151 574275429 622 TGA 629 633 163792200 1425 TAG 1542 574275427 622 TGA 629 633 119829186 1344 TAA 1374 574275776 622 TGA 629 633 119829186 1344 TGA 1363 574275778 557 TGA 564 568 305410830 1079 TAG 1111 169234948 317 TAG 360 370 284004924 591 TAA 593 169234948 317 TGA 336 370 224994180 967 TGA 974 557636701 3791 TAA 3834 3870 270483791 1363 TGA 1364 557636701 3791 TGA 3826 3870 305410832 747 TAG 780 344925844 1128 TGA 1241 1282 307746901 1016 TAG 1048 115298681 736 TGA 746 787 270132520 4540 TAA 4667 61743939 295 TAA 310 327 153791627 1121 TAG 1132 61743939 295 TAG 324 327 153791627 1121 TGA 1136 61743939 295 TGA 306 327 166235162 541 TAA 591 289547543 894 TAA 992 1033 193788631 841 TAG 883 7705934 473 TAG 718 750 193788631 841 TGA 857 209870072 451 TAA 514 559 194353965 6584 TAG 6589 209870078 917 TAA 979 1024 217330569 1221 TAG 1261 209870070 704 TAA 766 811 217330573 1408 TAG 1448 215599561 320 TAG 481 508 51873044 1026 TAG 1091 544583540 918 TAA 1032 1064 119395733 9174 TAG 9307 284172494 1574 TAA 1651 1685 217330567 1513 TAG 1553 239582713 995 TAG 1343 1371 51873046 1122 TAG 1187 225579094 2815 TAA 2826 2848 299782586 1712 TGA 1735 225579094 2815 TGA 2838 2848 289547522 1454 TAG 1494 110347419 1175 TAA 1181 1221 574269958 1379 TAA 1458 110347419 1175 TAG 1192 1221 574269958 1379 TAG 1385 110347419 1175 TGA 1187 1221 574272532 1583 TAA 1662 284795233 1121 TAG 1132 1149 574272532 1583 TAG 1589 284795233 1121 TGA 1136 1149 574272304 1192 TAA 1271 544583452 918 TAA 1032 1064 574272304 1192 TAG 1198 399498564 848 TAG 902 943 574271714 1478 TAA 1557 399498564 848 TGA 906 943 574271714 1478 TAG 1484 399498565 851 TAA 863 904 574271316 1379 TAA 1458 223005861 4124 TGA 4130 4134 574271316 1379 TAG 1385 155029543 670 TAG 810 848 574273241 1478 TAA 1557 155029541 801 TAG 941 979 574273241 1478 TAG 1484 157739935 1035 TAA 1036 1063 574269522 1427 TAA 1506 38202203 1157 TAA 1292 1305 574269522 1427 TAG 1433 388240807 1129 TAA 1135 1175 558472849 1026 TAG 1091 388240807 1129 TAG 1146 1175 156523967 855 TAA 867 388240807 1129 TGA 1141 1175 156523967 855 TAG 864 67782329 488 TAG 1321 1324 156523967 855 TGA 873 542133168 2773 TAA 2877 2887 112382209 1093 TAA 1108 542133168 2773 TAG 2838 2887 112382209 1093 TAG 1174 542133173 2334 TAA 2438 2448 112382209 1093 TGA 1097 542133173 2334 TAG 2399 2448 111120330 2052 TAA 2059 542133166 2690 TAA 2794 2804 111120330 2052 TAG 2224 542133166 2690 TAG 2755 2804 111120330 2052 TGA 2068 542133167 2827 TAA 2931 2941 88703042 692 TAA 713 542133167 2827 TAG 2892 2941 109255233 1177 TAG 1255 542133171 2646 TAA 2750 2760 88703040 587 TAA 608 542133171 2646 TAG 2711 2760 112789561 683 TGA 836 542133176 1321 TAA 1425 1435 126032349 10872 TAG 10941 542133176 1321 TAG 1386 1435 62244047 946 TAG 963 542133175 1388 TAA 1492 1502 226437633 186 TAA 452 542133175 1388 TAG 1453 1502 226437633 186 TAG 496 542133172 2571 TAA 2675 2685 226437633 186 TGA 209 542133172 2571 TAG 2636 2685 199559531 1216 TAA 1223 365192531 3074 TAA 3322 3354 189163519 4030 TAA 4062 239787905 1468 TAA 1543 1587 189163519 4030 TAG 4116 239787905 1468 TAG 1584 1587 189163519 4030 TGA 4051 239787905 1468 TGA 1557 1587 199559437 1154 TAA 1161 393185909 180 TAG 191 237 199559489 1301 TAA 1308 393185909 180 TGA 216 237 199558961 1216 TAA 1223 542133170 2639 TAA 2743 2753 205360986 300 TAA 372 542133170 2639 TAG 2704 2753 205360986 300 TAG 387 95147341 3226 TAA 3230 3264 205360986 300 TGA 304 95147341 3226 TAG 3238 3264 305410834 1016 TAG 1048 95147341 3226 TGA 3247 3264 32479524 1140 TAG 1659 34577113 1789 TAG 1857 1898 215982795 767 TAG 823 542133169 2639 TAA 2743 2753 349501056 1573 TAG 1613 542133169 2639 TAG 2704 2753 305410827 909 TAG 942 422398891 320 TAA 417 438 349501055 1573 TAG 1613 422398891 320 TAG 526 529 349501059 916 TAG 956 284795244 1103 TAG 1114 1131 349501060 1573 TAG 1613 284795244 1103 TGA 1118 1131 32479526 1373 TAG 1892 301500638 762 TAA 887 905 167860144 1425 TAA 1448 151301203 1982 TAA 2027 2050 167860144 1425 TGA 1473 151301203 1982 TGA 2030 2050 305410836 693 TAG 726 573459695 1552 TAA 1882 1906 386781570 946 TAG 963 422398886 320 TAA 417 438 167830435 2605 TGA 2714 296080784 530 TGA 663 703 167830432 658 TAG 857 300244517 499 TAA 535 547 167830432 658 TGA 660 300244517 499 TAG 517 547 594191052 1137 TAA 1416 300244517 499 TGA 502 547 594191052 1137 TAG 1236 296278216 1064 TAA 1146 1187 55956799 426 TAA 429 527317401 2486 TGA 2588 2594 113204614 8646 TAG 8716 313661424 3736 TGA 3751 3795 113204616 8646 TAG 8716 52145311 2119 TAA 2152 2183 296939603 2391 TAA 2823 52145311 2119 TGA 2139 2183 296939601 2391 TAA 2823 300797236 693 TAG 800 808 27765081 2101 TAA 2199 422398893 337 TAA 434 455 27765081 2101 TAG 2288 422398893 337 TAG 543 546 27765081 2101 TGA 2196 574274904 622 TGA 629 633 157266316 2444 TAA 2455 296278222 341 TAA 423 464 157266316 2444 TAG 2447 422398882 337 TAA 434 455 27765075 428 TAA 526 544346208 1454 TAG 1536 1580 27765075 428 TAG 615 544346208 1454 TGA 1623 1648 27765075 428 TGA 523 291084569 1795 TAG 2235 2249 207113159 4478 TGA 4515 291084569 1795 TGA 1825 1860 304376300 4364 TGA 4401 284795242 1103 TAG 1114 1131 207113158 4247 TGA 4284 284795242 1103 TGA 1118 1131 207113161 4367 TGA 4404 313661429 3451 TGA 3466 3510 207113163 4250 TGA 4287 324711032 1276 TAG 1294 1323 236463299 559 TAA 595 324711032 1276 TGA 1307 1323 236463299 559 TAG 574 313661427 3610 TGA 3625 3669 236463299 559 TGA 587 555943904 605 TAG 608 654 236463163 559 TAA 595 555943904 605 TGA 718 744 236463163 559 TAG 574 301500639 738 TAA 863 881 236463163 559 TGA 587 302191685 381 TAA 404 441 349501083 1110 TAG 1150 422398895 337 TAA 434 455 315360665 835 TAG 842 422398895 337 TAG 543 546 315360665 835 TGA 837 422398884 320 TAA 417 438 387527982 915 TAG 1058 422398884 320 TAG 544 547 387527982 915 TGA 929 300244513 239 TAA 275 287 402513678 237 TAA 246 300244513 239 TAG 257 287 402513678 237 TAG 257 300244513 239 TGA 242 287 305410841 927 TAG 959 313661433 3604 TGA 3619 3663 305410838 905 TAG 937 300244516 430 TAA 466 478 305410844 1074 TAG 1106 300244516 430 TAG 448 478 574957022 893 TAA 901 300244516 430 TGA 433 478 574957022 893 TAG 1028 527317400 2615 TGA 2717 2723 574957022 893 TGA 920 422398870 337 TAA 434 455 574957031 1965 TAA 1973 422398870 337 TAG 561 564 574957031 1965 TAG 2100 555943722 605 TAG 608 654 574957031 1965 TGA 1992 555943722 605 TGA 718 744 386268034 971 TAG 1012 284004933 616 TAA 618 625 386268035 971 TAG 1012 296278218 560 TAA 642 683 386268037 971 TAG 1012 574275184 577 TGA 584 588 223555916 1674 TAA 1693 574275536 666 TGA 673 677 223555916 1674 TGA 1687 386781586 575 TAG 592 638 396578113 1329 TAA 1399 300797255 693 TAG 800 808 396578113 1329 TGA 1452 386781549 946 TAG 963 1009 396578116 1117 TAA 1187 557947981 412 TAA 718 752 396578116 1117 TGA 1240 557947981 412 TGA 430 435 95147334 3551 TAA 3660 110347424 1113 TAA 1119 1159 160707983 2206 TAG 2264 110347424 1113 TAG 1130 1159 154146192 1034 TAA 1086 110347424 1113 TGA 1125 1159 154146192 1034 TGA 1050 110347417 1104 TAA 1110 1150 145275203 1841 TAA 1907 110347417 1104 TAG 1121 1150 154146222 954 TAA 1006 110347417 1104 TGA 1116 1150 154146222 954 TGA 970 53729338 2711 TAA 2714 2749 120953299 4732 TAG 4829 53729336 2290 TAA 2293 2328 120953299 4732 TGA 4784 94538369 841 TAG 883 905 189409139 1021 TAA 1074 94538369 841 TGA 857 905 189409139 1021 TAG 1096 160707983 2206 TAA 2238 2272 239787837 233 TAG 377

TABLE 3 shows a table showing peptides arising from possible frame-shifting on polyA tracks. Direction of frame-shift, gene name and peptide sequences following polyA track are shown in table. Additional analyses of possible eukaryotic linear motifs (ELMs) found in these peptides is included. Frameshift Gene name Sequence ELMs minus one ALS2CR12 TKKFEMESGEE ELME000117 ELME000085 ELME000064 minus one APTX LEFFQYRIL ELME000355 ELME000370 ELME000120 minus one ASTE1 EETEYQLF ELME000370 ELME000236 ELME000120 ELME000352 minus one BRCA1 QPNASQAQQKPTTHGR ELME000202 ELME000353 ELME000239 ELME000070 minus one C10orf90 RTKEKGDLTK ELME000351 minus one CASP5 DVLLYDTIFQIFNNRNCLS ELME000020 ELME000336 ELME000370 ELME000335 ELME000120 ELME000352 minus one CCDC146 SWNKKSKR ELME000011 ELME000285 ELME000278 minus one CCDC148 LGQEKTEVARNG ELME000355 minus one CCDC168 KKVSKLGSQGWRNQ ELME000202 ELME000351 ELME000008 ELME000053 minus one CDYL RQSIWFGGKA ELME000351 ELME000197 minus one CENPQ HLKDLSSEGQTKH ELME000334 ELME000053 minus one CEP290 HYQLQVOELTDL ELME000086 ELME000163 minus one CHEK1 YLNPWKKIDSAPLALL ELME000182 ELME000085 ELME000084 ELME000355 ELME000081 minus one CHRM5 EEKLYWQGNSKLP ELME000352 ELME000137 minus one CNTLN MLKMTRNGCCTFRNFLKDSFLLPHIY ELME000146 ELME000336 ELME000079 ELME000337 ELME000355 ELME000370 ELME000369 minus one CNTRL AAQTRLSEL ELME000086 ELME000285 minus one CPNE3 TRIQVLSV ELME000333 ELME000091 ELME000365 minus one DHX36 TFGILKCSISEKSCLRMECKRNW ELME000336 ELME000162 ELME000368 ELME000063 ELME000103 ELME000360 ELME000370 ELME000108 ELME000064 ELME000100 minus one DIAPH3 TDFFVLWKASGTIQFNCK ELME000368 ELME000085 ELME000370 ELME000328 minus one DYNC112 TRRRKLLLLCKKNQILKKKGEKLK ELME000146 ELME000149 ELME000106 HCFKAWG ELME000108 ELME000231 ELME000012 ELME000233 ELME000102 minus one EIF2AK2 LLQKLLSKK ELME000045 ELME000355 minus one FAM133A SKDETEKEKD ELME000285 ELME000220 ELME000064 minus one FBXO38 DVYPSCSSTTASTVGNSSSHNTASQS ELME000136 ELME000202 ELME000063 PDF ELME000159 ELME000197 ELME000239 ELME000070 ELME000352 ELME000053 minus one FILIP1 EILLLAQNEPCPQSQLLHFPERRLQKV ELME000202 ELME000173 ELME000335 EEAHLQTGPHPLFR ELME000108 ELME000012 ELME000352 ELME000102 minus one GON4L TKRKRDGRGQEGTLAYDLKLDDMLDR ELME000147 ELME000108 ELME000220 TLEDGAKQHN ELME000365 ELME000100 ELME000102 minus one GOPC KEAQLEAEVKLLRKENEAL ELME000232 ELME000351 ELME000335 ELME000365 ELME000089 ELME000102 minus one GPATCH4 KEAERGGRSYSI ELME000091 ELME000351 minus one HMGXB4 RRTKREREEKSQKRRTCRPTRCS ELME000271 ELME000202 ELME000101 ELME000351 ELME000062 ELME000108 ELME000220 ELME000276 ELME000100 ELME000008 ELME000102 ELME000053 minus one IFI16 PKKRLDPKG ELME000106 ELME000108 ELME000100 minus one IQCA1 EEEKGKTTQESQKTKERNKGEK ELME000117 ELME000202 ELME000063 ELME000220 ELME000064 ELME000352 ELME000053 minus one JARID2 SHSQYHLSPPG ELME000367 ELME000249 ELME000136 ELME000159 ELME000285 minus one KNOP1 HQEGDALPGHSKPSRSMESS ELME000063 ELME000287 ELME000239 ELME000053 minus one KRCC1 NKAKKGQRRKCFGTSLFLD ELME000336 ELME000353 ELME000108 ELME000102 minus one LPIN2 GERNTNRT ELME000062 minus one MAST4 SGKVTKSLSASALSLMIPGDMFAVSPL ELME000155 ELME000182 ELME000367 GSPMSPHSLSSDPSSSRDSSPSRDSS ELME000336 ELME000136 ELME000149 AASASPHQPIVIHSSGKNYGFTIRAIRV ELME000147 ELME000337 ELME000085 YVGDSDIYTVHHIVWNVEEGSPACQA ELME000063 ELME000159 ELME000173 GLKAGDLITHINGEPVHGLVHTEVIELLL ELME000335 ELME000062 ELME000285 KSG ELME000313 ELME000153 ELME000365 ELME000148 ELME000239 ELME000052 ELME000321 ELME000053 minus one MED19 KRILNGKGRRKRRRKRRIDIVQTTQVW ELME000271 ELME000146 ELME000202 AAPRPAAAAAY ELME000101 ELME000103 ELME000093 ELME000351 ELME000108 ELME000278 ELME000012 ELME000233 ELME000369 ELME000052 ELME000276 ELME000100 ELME000270 ELME000102 minus one MGA MGSDEFDISPRISKQQEGSSASSVDLG ELME000136 ELME000085 ELME000063 QMF ELME000159 ELME000062 ELME000365 ELME000197 ELME000053 minus one MIS18BP1 SIPTYVKKRKTTNHSSQMTVH ELME000182 ELME000271 ELME000202 ELME000063 ELME000062 ELME000285 ELME000108 ELME000070 ELME000100 ELME000008 ELME000270 ELME000102 ELME000053 minus one MKNK1 HQQPRACVY minus one MORC4 IITEDSLPSLEAILNYSIFNRENDLLAQF ELME000336 ELME000149 ELME000147 DAIPGKKGTRVLIWNIRR ELME000063 ELME000355 ELME000106 ELME000093 ELME000120 ELME000341 ELME000012 ELME000287 ELME000069 ELME000365 ELME000233 ELME000070 ELME000052 ELME000008 ELME000137 minus one MYH10 QAHIQDLEEQLDEEEGARQKLQLEKVT ELME000342 ELME000146 ELME000117 AEAKIKKMEEEILLLEDQNSKFIKEKKL ELME000149 ELME000202 ELME000106 MEDRIAECSSQLAEEEEKAKNLAKIR ELME000333 ELME000335 ELME000353 ELME000365 ELME000233 ELME000239 minus one NEK3 QQNQDSFGK ELME000353 minus one NGFRAP1 LIMANIHQENEEMEQPMQNGEEDRPL ELME000355 GG minus one NIPBL ILTHRRLGVLQE ELME000355 ELME000106 ELME000108 ELME000012 ELME000102 minus one NPIPB15 KTKQNPRSKNK ELME000351 minus one NR3C1 FSRPLQESHKKP ELME000117 ELME000336 ELME000355 minus one NUP85 RWCQVAPLSISS ELME000351 minus one OSBPL1A LSEALETLA ELME000086 ELME000355 minus one PA2G4 GLQDCRECHQWGNIRRK ELME000108 ELME000012 ELME000060 ELME000102 minus one PHLPP1 RRIHGQYIHCHAKETWNCWAEAWWC ELME000182 ELME000160 ELME000091 RCPLSYQA ELME000351 ELME000108 ELME000012 ELME000365 ELME000102 minus one PLXNC1 QILTSYIFGKQTAFLFASG ELME000182 ELME000198 ELME000353 ELME000197 ELME000052 minus one PPP1R10 CHLRLPSQAP ELME000354 ELME000367 ELME000202 ELME000334 minus one PRPF40A QAKQLRKRNWEA ELME000271 ELME000353 ELME000108 ELME000278 ELME000012 ELME000100 ELME000102 minus one PXK FSSKEVKTICS ELME000146 ELME000355 minus one RNF145 AAKEKLEAV ELME000285 ELME000365 ELME000089 minus one SENP7 YPRVSCYFQVITRKDTQSY ELME000182 ELME000368 ELME000337 ELME000202 ELME000370 ELME000062 ELME000120 ELME000220 ELME000365 ELME000197 ELME000239 ELME000008 ELME000102 ELME000053 minus one SGOL1 VPQKKMHKSVSS ELME000336 minus one SH3RF1 FVEVAFWRLH ELME000368 ELME000355 ELME000370 minus one SLC46A3 SPIFAFQEEVQKKVSR ELME000117 ELME000011 ELME000285 minus one SMAD5 CHGGTGESLEQSRTAE ELME000354 ELME000336 ELME000053 minus one SPATA16 ATSNCSAK ELME000085 ELME000285 ELME000070 minus one TAF1D RYQPTGRPRGRPEGRRNPIYS ELME000103 ELME000093 ELME000351 ELME000122 ELME000108 ELME000097 ELME000012 ELME000095 ELME000102 minus one TAOK1 SGFQSRRRIYSISKQKKK ELME000011 ELME000285 ELME000108 ELME000012 ELME000065 ELME000051 ELME000061 ELME000102 minus one TDRD5 HNRRFARS ELME000108 ELME000012 ELME000102 minus one TFDP2 SGLACLPILLRNVRIWR ELME000285 minus one TMEM254 KKIEAKNGDPNDCSEFLRSVWVVFWP ELME000020 ELME000155 ELME000182 QSIPYQNLGPLGPFTQYLVDHHHTLLC ELME000317 ELME000336 ELME000079 NGYWLAWLIHVGESLYAIVLCK ELME000368 ELME000160 ELME000202 ELME000084 ELME000351 ELME000370 ELME000335 ELME000120 ELME000081 ELME000052 minus one U2SURP IWNSSKKN ELME000355 ELME000070 minus one ULK4 RECWAVPLAAYTV ELME000091 ELME000351 ELME000369 minus one VEZF1 KLHLCALTA ELME000091 ELME000351 minus one ZC3H13 WKSQERENLGLIS ELME000149 ELME000355 ELME000333 ELME000231 minus one ZMYM5 IDAAEHRLYENEKNDGVLLLYT ELME000149 ELME000084 ELME000355 ELME000321 minus one ZRANB2 QRESSWSCIY ELME000080 ELME000199 ELME000368 ELME000147 ELME000063 ELME000370 ELME000062 ELME000353 plus one ABCC2 SLGPKKMFQNPG ELME000146 ELME000285 plus one ALS2CR12 MTKKFEMESGEE ELME000117 ELME000085 ELME000064 plus one ANKHD1- GTEKETGRR ELME000093 EIF4EBP3 plus one ANKHD1 GTEKETGRR ELME000093 plus one ANKRD49 GKRPKQIASLGC ELME000091 ELME000108 ELME000100 ELME000270 plus one APAF1 ITNLSRLVVRPHTDAVYHACF ELME000155 ELME000355 ELME000371 ELME000070 ELME000052 plus one APTX IGILSIQNTS ELME000355 ELME000333 ELME000053 plus one APTX WNSFNTEYF ELME000063 ELME000355 ELME000089 plus one BBX KKSKMDRHG ELME000351 plus one BEND2 YQPCCIGICR ELME000355 plus one BLM VSSKSVSEGRDG ELME000063 ELME000064 ELME000321 plus one BRCA1 YNQMPVRHSRNLQLME ELME000355 ELME000106 ELME000062 ELME000120 plus one C10orf90 RTKEKGDLTK ELME000351 plus one C16orf45 KLOKQREDE ELME000351 plus one CAPN3 SPSSSFRTEQTATRSWVWTRSQRRAK ELME000146 ELME000011 ELME000147 AKQA ELME000337 ELME000202 ELME000063 ELME000285 ELME000108 ELME000365 ELME000197 ELME000239 ELME000102 ELME000053 plus one CASP5 DVLLYDTIFQIFNNRNCLS ELME000020 ELME000336 ELME000370 ELME000335 ELME000120 ELME000352 plus one CASP5 RMCCFMTPSSRYSTTATASV ELME000358 ELME000136 ELME000063 ELME000159 ELME000351 ELME000062 ELME000365 ELME000239 ELME000053 plus one CCDC122 VLFNLKNELHELEKEIAAISAE ELME000085 ELME000002 ELME000365 plus one CCDC146 CLGTRSQN ELME000354 plus one CCDC148 WAKKKQKWQEME ELME000271 ELME000201 ELME000355 ELME000278 plus one CEP290 IIINFKCRSLQIF ELME000355 ELME000106 plus one CHD9 RRRYRREAI ELME000101 ELME000103 ELME000351 ELME000108 ELME000012 ELME000089 ELME000102 plus one CHRM5 WKRSCTGRGTASY ELME000355 ELME000173 ELME000062 ELME000108 ELME000100 ELME000053 plus one CNTRL QHKLDYQNC ELME000084 ELME000353 plus one EIF2AK2 FYRNYSQRN ELME000202 ELME000084 ELME000355 ELME000070 plus one EIF5B TEGOKTEF ELME000086 plus one ERC2 ATGPHRREGDTGR ELME000285 ELME000108 ELME000102 plus one ERO1LB ARERLFSLLQG ELME000045 ELME000368 ELME000149 ELME000370 ELME000285 ELME000231 ELME000061 plus one EXOC1 NCFLCATVTTERPVQ ELME000336 ELME000353 plus one FAM133A SQRMKQRKKRM ELME000271 ELME000011 ELME000101 ELME000285 ELME000108 ELME000100 ELME000270 ELME000102 plus one FAM227B DSSFVSIYTHLWENVPRIFEALLIMESK ELME000182 ELME000368 ELME000063 ELME000370 ELME000120 ELME000047 ELME000365 ELME000352 plus one FAM81 B TEIVFQKYQIYKK ELME000370 plus one FILIP1 WRYYSWPRTSHVPSHNYYIFQREDSR ELME000182 ELME000271 ELME000355 KWKRRICRQAHIPYS ELME000103 ELME000370 ELME000062 ELME000120 ELME000108 ELME000278 ELME000012 ELME000048 ELME000239 ELME000052 ELME000100 ELME000163 ELME000102 ELME000053 plus one FOXP3 MRTPPHPVIISAHTHRKKFGLLEERGL ELME000358 ELME000155 ELME000367 RLPHRTAWFFFSV ELME000085 ELME000063 ELME000106 ELME000333 ELME000091 ELME000351 ELME000370 ELME000365 ELME000102 plus one GGNBP2 KKKKSKILKCDEHIQKLGSCITDP ELME000271 ELME000146 ELME000007 ELME000351 ELME000173 ELME000278 ELME000008 plus one GYPC GVETPPAKSAEKK ELME000358 ELME000136 ELME000085 ELME000159 ELME000239 plus one HMGXB4 REGQRERERRKAKKEEHVGLPGVL ELME000155 ELME000271 ELME000146 ELME000101 ELME000103 ELME000351 ELME000108 ELME000002 ELME000278 ELME000233 ELME000102 plus one HYDIN EIESDFLATTNTTKAQEEQTSS ELME000117 ELME000336 ELME000070 ELME000352 ELME000053 plus one IGHMBP2 QRTSGHRSAHGGGL ELME000085 ELME000062 ELME000353 ELME000053 plus one IL1R2 DHSCDHFPPQDHISFSGVKTDNPV ELME000368 ELME000085 ELME000370 ELME000352 ELME000053 plus one IQCA1 KKKKKEKQPKKAKKQKKGTKEK ELME000271 ELME000146 ELME000351 ELME000278 ELME000276 ELME000008 plus one JARID2 GPTLSTISALL ELME000085 ELME000063 ELME000365 plus one KCNC1 KHIPRPPQLGSPNY ELME000155 ELME000199 ELME000136 ELME000159 ELME000351 ELME000005 plus one KDM4D HDCGGVSPFGKQ ELME000136 ELME000159 plus one KNOP1 TRREMPSQATPSPPGPWRAA ELME000358 ELME000155 ELME000006 ELME000136 ELME000202 ELME000063 ELME000159 ELME000108 ELME000102 plus one LARP7 DRVEASSLPEVRTGKRKRSSSEDAES ELME000271 ELME000093 ELME000173 LAPRSK ELME000062 ELME000108 ELME000365 ELME000064 ELME000100 ELME000061 ELME000008 ELME000352 ELME000270 ELME000102 plus one LOC101929870 QKSFPSEGQRQRRSLFLDSNSRENLG ELME000146 ELME000336 ELME000085 WLAKLTREQNILPEAEKPHALSGGG ELME000063 ELME000101 ELME000106 ELME000062 ELME000353 ELME000108 ELME000231 ELME000012 ELME000365 ELME000233 ELME000051 ELME000102 plus one LPIN2 KEKEIQTGQ ELME000351 plus one MPP3 PPMSPACEDTAAPFDEQQQEMAASAA ELME000146 ELME000336 ELME000136 FIDRHYGHLVDAVLVKEDLQGAYSQLK ELME000368 ELME000147 ELME000202 VVLEKLSKDTHWVPVSWVR ELME000085 ELME000063 ELME000159 ELME000333 ELME000370 ELME000120 ELME000326 ELME000313 ELME000365 ELME000197 ELME000233 ELME000052 plus one NAA35 SPIEPRDHNEPSISEHVCWNV ELME000147 ELME000285 ELME000365 ELME000064 plus one NCOA7 SQTKCRDSLSCSYKDSYWEGR ELME000336 ELME000162 ELME000062 ELME000285 ELME000064 ELME000321 ELME000053 plus one NEK3 PSRIRIALG ELME000146 ELME000012 ELME000365 plus one NHLRC2 CTTLAGTGDT ELME000354 plus one NIPBL KKRKAYEPK ELME000271 ELME000351 ELME000108 ELME000278 ELME000100 ELME000102 plus one NIPBL RFLPTGGWGCYRR ELME000106 ELME000351 ELME000370 ELME000012 plus one NPIPB15 KKQNKTHAPKTN ELME000351 ELME000070 plus one NR3C1 NSAGHYRSLTRNL ELME000146 ELME000085 ELME000353 ELME000120 ELME000334 plus one OSBPL1A CQKHWRRWP ELME000354 ELME000160 ELME000108 ELME000012 ELME000102 plus one PDZD9 ERGVSNKVKTSVHNLSKTQQTKLTV ELME000336 ELME000202 ELME000091 ELME000365 ELME000070 ELME000352 plus one PEG10 GVEEGARIQASIPTE ELME000365 ELME000051 ELME000060 plus one PPFIA2 RLGQLRGFMETEAAAQESLG ELME000117 ELME000351 ELME000140 ELME000239 plus one PPP1R10 TVTYGCQAKPL ELME000163 plus one PRR14L CEENVCRS ELME000354 ELME000079 plus one QTRTD1 LGKTGDHTMDIPGCLLYTKTGSAPHLT ELME000182 ELME000336 ELME000147 HHTL ELME000085 ELME000355 ELME000173 ELME000052 ELME000053 plus one RALGPS2 SSAPNAVAFTRRFNH ELME000085 ELME000285 ELME000328 ELME000108 ELME000012 ELME000102 plus one RBPJ MERDGCSEQESQPCAFIG ELME000117 ELME000202 ELME000064 ELME000352 ELME000053 plus one RNF10 RNRSSCSAPQSSTP ELME000085 ELME000063 ELME000351 ELME000062 ELME000239 ELME000070 ELME000053 plus one RNF145 WLQRRNWRQC ELME000355 ELME000108 ELME000102 plus one RYR1 RKISQSAQT ELME000202 ELME000085 ELME000351 ELME000008 plus one SENP7 HIRGCPVTSKSSPERQLKVMLTNVLWT ELME000146 ELME000336 ELME000136 DLGRKFRKTLPRND ELME000063 ELME000106 ELME000159 ELME000093 ELME000062 ELME000153 ELME000278 ELME000365 ELME000064 ELME000239 ELME000052 ELME000102 ELME000053 plus one SENP7 YPRVSCYFQVITRKGLTTK ELME000182 ELME000146 ELME000368 ELME000337 ELME000370 ELME000062 ELME000120 ELME000365 ELME000197 ELME000239 ELME000102 plus one SGOL1 FPKKKCTNLSVP ELME000271 ELME000367 ELME000365 ELME000233 ELME000070 ELME000008 plus one SLC26A8 KKGPERAPFLVSFVQ ELME000336 ELME000149 ELME000351 ELME000328 plus one SLC46A3 AQFLHSRRKFRKKCHV ELME000271 ELME000336 ELME000011 ELME000285 ELME000108 ELME000278 ELME000102 plus one SLC4A7 KEEAERMLQDDDDTVHLPFEGGSLLQI ELME000155 ELME000367 ELME000149 PVKA ELME000147 ELME000091 ELME000351 ELME000335 ELME000240 ELME000052 plus one SLCO5A1 SVDAVSDDDVLKEKSNNSEQADKKVS ELME000063 ELME000106 ELME000091 SMGFGKDVRDLPRAAVRI ELME000198 ELME000285 ELME000365 ELME000197 ELME000233 ELME000070 ELME000008 plus one SLCO5A1 SVDAVSDDDVLKEKSNNSEQADKKVS ELME000085 ELME000063 ELME000198 SMGFGKDVRGVIIVPSAGVGIVLGGYI ELME000285 ELME000365 ELME000197 ELME000233 ELME000070 ELME000008 plus one SPG11 IFLKKRKEL ELME000011 ELME000355 ELME000108 ELME000100 ELME000102 plus one SYCP1 QENTNIFIGNT ELME000353 plus one TCF25 EKQEKQHGRSIGKRTRRYRSHPRED ELME000101 ELME000103 ELME000093 ELME000108 ELME000278 ELME000012 ELME000048 ELME000100 ELME000352 ELME000102 plus one TDRD5 ATTEDLQEA ELME000285 ELME000052 plus one TERF1 SRRATESRIPVSKSQP ELME000146 ELME000062 ELME000285 ELME000108 ELME000239 ELME000008 ELME000102 plus one TFDP2 QVDWPAYQFCSGMSESG ELME000085 ELME000063 ELME000370 ELME000353 plus one THOC2 KERCTALQDKLLEEEKKOMEHVORVL ELME000351 ELME000062 ELME000002 QRLKLEKDNWL plus one TMEM254 KENRSQEWRPK ELME000202 ELME000351 ELME000070 plus one TNRC6B ATQKVTEQKTKVPE ELME000011 ELME000285 ELME000053 plus one TRAPPC10 QHPSPNLYCGQ ELME000182 ELME000136 ELME000159 ELME000353 ELME000163 plus one TRDN CRSRTTQGKKTGKERKTCGTSKVTKE ELME000354 ELME000147 ELME000202 RTLRN ELME000063 ELME000093 ELME000173 ELME000062 ELME000220 ELME000064 ELME000052 ELME000102 ELME000053 plus one TRDN RNKDTGERTEES ELME000351 ELME000053 plus one TRPC1 IASGIPGFVLIYIDVWPVQL ELME000020 ELME000182 ELME000085 ELME000355 ELME000333 ELME000091 ELME000120 ELME000083 ELME000047 ELME000365 ELME000081 plus one ULK4 LESAGLFPWLHTQC ELME000086 ELME000085 ELME000355 plus one VEZF1 QNFICVHLLQ ELME000353 plus one WNK1 QEESSLKQQVEQSSASQTGIKQLPSAS ELME000147 ELME000202 ELME000085 TGIPTASTTSASVSTQVE ELME000063 ELME000106 ELME000353 ELME000365 ELME000064 ELME000239 ELME000053 plus one ZCRB1 LLNQKKKLRK ELME000271 ELME000011 ELME000355 ELME000278 ELME000102 plus one ZDHHC3 DEHESRFWPPLLSRLGQPLCHARPRE ELME000136 ELME000368 ELME000063 GRPVPVCGLKDPDRHGHSDTSPHHST ELME000159 ELME000370 ELME000173 TVPSVLMNV ELME000365 ELME000233 ELME000239 ELME000369 ELME000352 ELME000053 plus one ZFHX3 STPFSFHS ELME000285 plus one ZMYM5 LLMLQNTDYMKMRKMMVCCCCT ELME000355 ELME000122 ELME000120 ELME000095 ELME000102

In conclusion, the presently disclosed subject matter demonstrates that lysine coding poly(A) nucleotide tracks in human genes act as translational attenuators. It is shown that the effect is dependent on nucleotide, not amino acid sequence, and the attenuation occurs in a distinct manner from previously described polybasic amino acid runs. These “poly(A) translational attenuators” are highly conserved across vertebrates, implying that they might play an important role in balancing gene dosage. Presence of such a regulatory function is further supported by negative selection against single nucleotide variants in human poly(A) segments both in dbSNP and COSMIC databases (FIG. 23 ; Table 4; Based on dbSNP data, it was found that variations in polyA region are less common than in randomly chosen section of the same length in genes that do not contain polyA segment (1,8k segments vs 71k segments, one random all transcripts, mean of 0.44 vs 0.49 variations per segment, p-value 0.008 with permutation test and 0.009 with Welch t-test). Almost 300 genes from the original set of 456 had no variation within polyA segment reported in dbSNP). However, it is not yet clear what the effects stemming from synonymous mutation in poly(A) tracks are. Results point to either alterations in protein-levels (altered gene dosage) or to the production of frame-shifted products in the cell. As such, these translational attenuation mechanisms may supplement the already large number of mechanisms through which synonymous mutations can exert biological effects (reviewed in Hunt et al. (2014) Trends Genet. TIG. 30, 308-321).

TABLE 4 Shows a table of genes with mutations within the polyA region reported in the COSMIC database. Gene name mutation (nucleotide) mutation (protein) Type of mutation AASDH c.342delA p.K114fs*14 Deletion - Frameshift ABCA5 c.733G > A p.E245K Substitution - Missense ABCA5 c.742_743insA p.I248fs*12 Insertion - Frameshift ABCA5 c.742A > T p.I248L Substitution - Missense ABCA5 c.742delA p.I248fs*1 Deletion - Frameshift ABCC2 c.882G > C p.K294N Substitution - Missense ACBD3 c.568delA p.R190fs*43 Deletion - Frameshift ADAL c.644delA p.E218fs*33 Deletion - Frameshift ADAL_ENST00000428046 c.563delA p.E191fs*33 Deletion - Frameshift AHI1 c.910_911insA p.T304fs*6 Insertion - Frameshift AHI1 c.910delA p.T304fs*23 Deletion - Frameshift AHI1 c.911C > A p.T304K Substitution - Missense AIM2 c.1027A > C p.T343P Substitution - Missense AIM2 c.1027delA p.T343fs? Deletion - Frameshift AKD1_ENST00000424296 c.2091A > G p.K697K Substitution - coding silent AKD1_ENST00000424296 c.2098_2099delGA p.E700fs*33 Deletion - Frameshift AKD1_ENST00000424296 c.2098G > A p.E700K Substitution - Missense AL118506.1 c.48G > A p.K16K Substitution - coding silent ALS2CR12 c.777A > C p.K259N Substitution - Missense ALS2CR12 c.778A > G p.K260E Substitution - Missense ANKHD1 c.4385A > G p.K1462R Substitution - Missense ANKHD1 c.4386G > A p.K1462K Substitution - coding silent ANKHD1-EIF4EBP3 c.4385A > G p.K1462R Substitution - Missense ANKHD1-EIF4EBP3 c.4386G > A p.K1462K Substitution - coding silent ANKRD12 c.2806_2809delAAAC p.K936fs*22 Deletion - Frameshift ANKRD1 c.215_216insA p.K73fs*10 Insertion - Frameshift ANKRD1 c.216G > T p.K72N Substitution - Missense ANKRD1 c.223C > T p.L75L Substitution - coding silent ANKRD26 c.1340_1341insA p.N447fs*5 Insertion - Frameshift ANKRD32_ENST00000265140 c.987A > C p.E329D Substitution - Missense ANKRD36C c.2517_2518insA p.Q840fs*11 Insertion - Frameshift ANKRD36C c.2713A > G p.K905E Substitution - Missense ANKRD36C c.2716T > C p.C906R Substitution - Missense ANKRD36C_ENST00000420871 c.2517_2518insA p.Q840fs*11 Insertion - Frameshift ANKRD36C_ENST00000420871 c.2713A > G p.K905E Substitution - Missense ANKRD36C_ENST00000420871 c.2716T > C p.C906R Substitution - Missense ANKRD49 c.200delA p.M70fs*32 Deletion - Frameshift APAF1 c.1798_1799delAA p.N602fs*23 Deletion - Frameshift APAF1 c.1798delA p.N602fs*8 Deletion - Frameshift APAF1 c.1799A > G p.K600R Substitution - Missense ARHGAP18 c.1418T > G p.M473R Substitution - Missense ARHGAP18 c.492delA p.K164fs*54 Deletion - Frameshift ASH1L c.2134delA p.R712fs*23 Deletion - Frameshift ASTE1 c.1884_1885delAA p.R632fs*10 Deletion - Frameshift ASTE1 c.1892A > G p.K631R Substitution - Missense ASTE1 c.1894_1895insA p.R632fs*11 Insertion - Frameshift ASTE1 c.1894delA p.R632fs*33 Deletion - Frameshift ATAD2 c.354_355insA p.E119fs*18 Insertion - Frameshift ATAD2 c.354delA p.E119fs*8 Deletion - Frameshift ATL1 c.1665G > T p.K555N Substitution - Missense ATR c.2320_2321insA p.I774fs*3 Insertion - Frameshift ATR c.2320delA p.I774fs*5 Deletion - Frameshift BARD1 c.623_624insA p.K209fs*5 Insertion - Frameshift BARD1 c.623delA p.K208fs*4 Deletion - Frameshift BARD1_ENST00000260947 c.623_624insA p.K209fs*5 Insertion - Frameshift BARD1_ENST00000260947 c.623delA p.K208fs*4 Deletion - Frameshift BAT2D1 c.464delA p.E158fs*66 Deletion - Frameshift BAT2D1_ENST00000392078 c.464delA p.E158fs*66 Deletion - Frameshift BEND5 c.545A > G p.K182R Substitution - Missense BEND5 c.545delA p.K182fs*15 Deletion - Frameshift BEND5 c.546G > A p.K182K Substitution - coding silent BEND5_ENST00000371833 c.1052A > G p.K351R Substitution - Missense BEND5_ENST00000371833 c.1052delA p.K351fs*15 Deletion - Frameshift BEND5_ENST00000371833 c.1053G > A p.K351K Substitution - coding silent BPTF c.2874delA p.I961fs*1 Deletion - Frameshift BPTF_ENST00000335221 c.3252delA p.I1087fs*1 Deletion - Frameshift BRCA1 c.1960_1961insA p.Y655fs*18 Insertion - Frameshift BRCA1 c.1961_1961delA p.K654fs*47 Deletion - Frameshift BRCA1 c.1961_1962insA p.Y655fs*18 Insertion - Frameshift BRCA1 c.1961delA p.K654fs*47 Deletion - Frameshift BRCA1_ENST00000471181 c.1961delA p.K654fs*47 Deletion - Frameshift BRCA2 c.8941G > A p.E2981K Substitution - Missense C10orf68 c.555G > A p.K185K Substitution - coding silent C10orf6 c.1002A > G p.E334E Substitution - coding silent C10orf90 c.1991A > T p.K664M Substitution - Missense C10orf90 c.1992_1993GA > TT p.K664_K665 > N* Complex - compound substitution C10orf90 c.1998delA p.E667fs*7 Deletion - Frameshift C10orf96 c.605A > C p.E202A Substitution - Missense C12orf45 c.544delA p.K184fs* > 2 Deletion - Frameshift C13orf40 c.2236_2237insA p.I746fs*40 Insertion - Frameshift C13orf40 c.2236delA p.I746fs*l Deletion - Frameshift C14orf102 c.261G > T p.K87N Substitution - Missense C14orf102 c.268_269insA p.R90fs*7 Insertion - Frameshift C14orf102 c.268delA p.R90fs*69 Deletion - Frameshift C14orf23 c.342_343insA p.T117fs*20 Insertion - Frameshift C14orf23 c.342delA p.T117fs*8 Deletion - Frameshift C14orf23 c.345A > C p.K115N Substitution - Missense C14orf23 c.346_347insAAC p.K116_T117insQ Insertion - In frame C14orf38 c.1890A > G p.K630K Substitution - coding silent C14orf38 c.1894_1895insA p.N632fs*6 Insertion - Frameshift C14orf38 c.1895_1896insA p.N632fs*6 Insertion - Frameshift C16orf45 c.310G > T p.E104* Substitution - Nonsense C16orf45 c.317C > A p.T106N Substitution - Missense C16orf88 c.647A > C p.K216T Substitution - Missense C16orf88 c.652delA p.I218fs*41 Deletion - Frameshift C18orf34 c.874delA p.M292fs*3 Deletion - Frameshift C18orf34_ENST00000383096 c.874delA p.M292fs*3 Deletion - Frameshift C1orf131 c.416G > A p.R139K Substitution - Missense C1orf9 c.850G > T p.E284* Substitution - Nonsense C1orf9_ENST00000367723 c.1327G > T p.E443* Substitution - Nonsense C2orf77 c.407A > G p.K136R Substitution - Missense C2orf77_ENST00000447353 c.407A > G p.K136R Substitution - Missense C3orf77 c.1885delA p.A632fs*5 Deletion - Frameshift C3orf77_ENST00000309765 c.1885delA p.A632fs*5 Deletion - Frameshift C6orf103_ENST00000367493 c.1813delA p.K607fs* > 6 Deletion - Frameshift C6orf10 c.1543G > A p.E515K Substitution - Missense CAMKK2_ENST00000392474 c.1601C > A p.T534K Substitution - Missense CAMSAP1L1 c.3748_3749insA p.Q1253fs*12 Insertion - Frameshift CAMSAP1L1 c.3749delA p.K1252fs*19 Deletion - Frameshift CAPN3_ENST00000397163 c.1788_1789insA p.T599fs*33 Insertion - Frameshift CASP5 c.153_154delAA p.K51fs*3 Deletion - Frameshift CASP5 c.154delA p.T52fs*26 Deletion - Frameshift CASP5_ENST00000393141 c.240_241delAA p.K80fs*3 Deletion - Frameshift CASP5_ENST00000393141 c.241delA p.T81fs*26 Deletion - Frameshift CCBL1_ENST00000427720 c.375_376delAA p.K125fs* > 34 Deletion - Frameshift CCDC108_ENST00000295729 c.438delA p.K146fs*3 Deletion - Frameshift CCDC148 c.1260delA p.K420fs*15 Deletion - Frameshift CCDC150 c.838_839insA p.E284fs*13 Insertion - Frameshift CCDC150 c.839delA p.E284fs*14 Deletion - Frameshift CCDC150 c.847A > G p.K283E Substitution - Missense CCDC150 c.850G > A p.E284K Substitution - Missense CCDC175 c.1890A > G p.K630K Substitution - coding silent CCDC34_ENST00000328697 c.720A > G p.L240L Substitution - coding silent CCDC34_ENST00000328697 c.731_732insA p.N244fs*3 Insertion - Frameshift CCDC34_ENST00000328697 c.731delA p.N244fs*28 Deletion - Frameshift CCT8L1 c.1642_1643insA p.I552fs*6 Insertion - Frameshift CCT8L2 c.1654_1655insA p.I552fs*6 Insertion - Frameshift CCT8L2 c.1654delA p.I552fs*4 Deletion - Frameshift CD46 c.509A > G p.N170S Substitution - Missense CDHR3_ENST00000542731 c.2259 − 2dela p.? Unknown CDKL2 c.222_223insA p.R75fs*7 Insertion - Frameshift CDKL2 c.222delA p.K74fs*5 Deletion - Frameshift CDYL c.216_217insA p.G75fs*13 Insertion - Frameshift CDYL c.217delA p.K76fs*25 Deletion - Frameshift CDYL c.219A > G p.K73K Substitution - coding silent CEP164 c.336_337insA p.E117fs*88 Insertion - Frameshift CEP164 c.337delA p.K116fs*22 Deletion - Frameshift CEP164 c.347A > G p.K116R Substitution - Missense CEP290 c.828delA p.E277fs*16 Deletion - Frameshift CHD2 c.3724_3725insA p.Y1246fs*13 Insertion - Frameshift CHD2 c.3725delA p.K1245fs*4 Deletion - Frameshift CHD2_ENST00000394196 c.3725delA p.K1245fs*4 Deletion - Frameshift CHD7 c.1922A > T p.K641I Substitution - Missense CHD7_ENST00000423902 c.1922A > T p.K641I Substitution - Missense CHEK1 c.668A > C p.E223A Substitution - Missense CHEK1 c.668delA p.T226fs*14 Deletion - Frameshift CHEK1 c.675A > G p.K225K Substitution - coding silent CIR1 c.865delA p.I289fs*51 Deletion - Frameshift CNTRL_ENST00000373855 c.1328delA p.I446fs*1 Deletion - Frameshift COL17A1 c.1170delA p.E391fs*12 Deletion - Frameshift COL17A1 c.1171G > C p.E391Q Substitution - Missense CPNE3 c.771G > A p.K257K Substitution - coding silent CPNE3 c.771G > T p.K257N Substitution - Missense CWC27 c.995delA p.V335fs*1 Deletion - Frameshift CWF19L2_ENST00000282251 c.279G > T p.K93N Substitution - Missense CWF19L2_ENST00000282251 c.287delA p.K96fs*41 Deletion - Frameshift DCLRE1C c.1706A > C p.K569T Substitution - Missense DCLRE1C c.1708delA p.R570fs*6 Deletion - Frameshift DCLRE1C_ENST00000378278 c.2051A > C p.K684T Substitution - Missense DCLRE1C_ENST00000378278 c.2053delA p.R685fs*6 Deletion - Frameshift DDX18 c.327G > T p.K109N Substitution - Missense DDX18 c.333G > T p.K111N Substitution - Missense DDX59 c.1294A > G p.K432E Substitution - Missense DDX59_ENST00000331314 c.1294A > G p.K432E Substitution - Missense DENR c.317delA p.K108fs*10 Deletion - Frameshift DHX36 c.2560delA p.R854fs*4 Deletion - Frameshift DHX36 c.2564A > T p.K855I Substitution - Missense DHX36 c.460_461insA p.M154fs*3 Insertion - Frameshift DHX36 c.460delA p.M154fs*27 Deletion - Frameshift DHX36 c.461_462insA p.M154fs*3 Insertion - Frameshift DHX36 c.578delA p.N193fs*25 Deletion - Frameshift DIAPH2 c.208G > T p.E70* Substitution - Nonsense DIAPH3 c.952A > C p.K318Q Substitution - Missense DIAPH3 c.958delA p.I320fs*20 Deletion - Frameshift DNAH6 c.6440G > T p.R2147I Substitution - Missense DNAJC1 c.578_579insA p.T194fs*18 Insertion - Frameshift DNAJC2 c.590_591insA p.N197fs*4 Insertion - Frameshift DNAJC2 c.590delA p.N197fs*8 Deletion - Frameshift DSEL c.2905_2906insA p.R969fs*4 Insertion - Frameshift DSEL c.2905delA p.R969fs*16 Deletion - Frameshift DSEL c.2910A > C p.K970N Substitution - Missense DSEL c.2910A > T p.K970N Substitution - Missense DYNC1I2 c.97delA p.E36fs*34 Deletion - Frameshift DYNC2H1_ENST00000398093 c.832A > C p.N278H Substitution - Missense EEA1 c.2428A > C p.K810Q Substitution - Missense EFCAB7 c.1138_1139insA p.I380fs*7 Insertion - Frameshift EHBP1 c.1026delA p.N344fs*2 Deletion - Frameshift EIF2AK2 c.1531G > T p.E511* Substitution - Nonsense EIF3J c.222G > C p.K74N Substitution - Missense EIF3J c.223delA p.I77fs*1 Deletion - Frameshift EIF3J c.229delA p.I77fs*1 Deletion - Frameshift EML6 c.4063delA p.K1357fs*9 Deletion - Frameshift EML6 c.4071G > T p.K1357N Substitution - Missense ENSG00000121031 c.10811delA p.N3604fs*48 Deletion - Frameshift ENSG00000121031 c.496_497insA p.I166fs*11 Insertion - Frameshift ENSG00000121031 c.496delA p.I166fs*6 Deletion - Frameshift ENSG00000174501 c.4764_4765insA p.Q1589fs*11 Insertion - Frameshift ENSG00000174501 c.4960A > G p.K1654E Substitution - Missense ENSG00000174501 c.4963T > C p.C1655R Substitution - Missense ENSG00000188423 c.651A > G p.K217K Substitution - coding silent ENSG00000188423 c.658_659delGA p.E220fs*33 Deletion - Frameshift ENSG00000188423 c.658G > A p.E220K Substitution - Missense ENSG00000225516 c.313A > C p.K105Q Substitution - Missense ENSG00000268852 c.52A > T p.K18* Substitution - Nonsense ERC2 c.1528delA p.T510fs*21 Deletion - Frameshift ERC2_ENST00000288221 c.1528delA p.T510fs*21 Deletion - Frameshift ERCC4 c.1461G > C p.K487N Substitution - Missense ERICH1 c.487delA p.R163fs*3 Deletion - Frameshift ERO1LB c.188A > C p.K63T Substitution - Missense ESCO2 c.1117G > C p.D373H Substitution - Missense F5 c.3096G > C p.K1032N Substitution - Missense F5 c.3102A > C p.K1034N Substitution - Missense F8 c.3632A > C p.K1211T Substitution - Missense F8 c.3637delA p.I1213fs*5 Deletion - Frameshift F8 c.3638T > G p.I1213S Substitution - Missense F8_ENST00000360256 c.3632A > C p.K1211T Substitution - Missense F8_ENST00000360256 c.3637delA p.I1213fs*5 Deletion - Frameshift F8_ENST00000360256 c.3638T > G p.I1213S Substitution - Missense FAM133A c.150T > G p.N50K Substitution - Missense FAM178A c.1002A > G p.E334E Substitution - coding silent FAM186A_ENST00000327337 c.2261delA p.K754fs*2 Deletion - Frameshift FAM200B c.170_173delAAGT p.S59fs*9 Deletion - Frameshift FAM200B_ENST00000422728 c.170_173delAAGT p.S59fs*9 Deletion - Frameshift FAM83A_ENST00000536633 c.1065delA p.K357fs*8 Deletion - Frameshift FAM9A c.477_478insA p.Q160fs*8 Insertion - Frameshift FAM9A c.477delA p.K159fs*3 Deletion - Frameshift FAM9A c.480A > G p.Q160Q Substitution - coding silent FASTKD1 c.2213G > T p.R738I Substitution - Missense FASTKD1 c.2216A > G p.K739R Substitution - Missense FASTKD1 c.2220delA p.K740fs*10 Deletion - Frameshift FAT4 c.12401delA p.K4136fs*17 Deletion - Frameshift FBXO38 c.2083delA p.N697fs*32 Deletion - Frameshift FBXO38 c.2085A > G p.K695K Substitution - coding silent FERMT2 c.452A > C p.K151T Substitution - Missense FERMT2 c.455delA p.K152fs*4 Deletion - Frameshift FERMT2 c.456G > A p.K152K Substitution - coding silent FERMT2 c.456G > AG p.K153fs*5 Complex - frameshift FEZ2 c.837G > T p.K279N Substitution - Missense FEZ2 c.838A > G p.K280E Substitution - Missense FLG c.476_477insA p.E160fs*10 Insertion - Frameshift FLG c.477_478insA p.E160fs*10 Insertion - Frameshift FLI45831 c.312G > T p.K104N Substitution - Missense FRA10AC1 c.694_695insA p.R232fs*4 Insertion - Frameshift FRA10AC1 c.694delA p.R232fs* > 84 Deletion - Frameshift FRA10AC1_ENST00000371426 c.694_695insA p.R232fs*4 Insertion - Frameshift FRA10AC1_ENST00000371426 c.694delA p.R232fs*67 Deletion - Frameshift GIMAP7 c.776delA p.I261fs*1 Deletion - Frameshift GOLGA4 c.4091delA p.V1367fs*10 Deletion - Frameshift GPR110 c.95_96insA p.E33fs*6 Insertion - Frameshift GPR110 c.95_96insT p.K32fs*7 Insertion - Frameshift GPR110_ENST00000371243 c.95_96insA p.E33fs*6 Insertion - Frameshift GRK4_ENST00000398052 c.656delA p.R222fs*2 Deletion - Frameshift GRK4_ENST00000398052 c.666_669delAATA p.I223fs*10 Deletion - Frameshift GRK4_ENST00000398052 c.668T > A p.I223K Substitution - Missense GRLF1 c.570A > T p.K190N Substitution - Missense GRLF1_ENST00000317082 c.570A > T p.K190N Substitution - Missense GRLF1_ENST00000317082 c.578A > C p.K193T Substitution - Missense HELLS c.454delA p.N154fs*29 Deletion - Frameshift HERC5 c.409_410insA p.I140fs*19 Insertion - Frameshift HERC5 c.410delA p.I140fs*1 Deletion - Frameshift HERC5 c.416A > T p.K139I Substitution - Missense HMGXB4 c.1163delA p.K391fs*33 Deletion - Frameshift HMGXB4 c.1173G > A p.K391K Substitution - coding silent HMMR c.1990_1991delAA p.K666fs*3 Deletion - Frameshift HMMR c.1990delA p.K666fs*11 Deletion - Frameshift IQGAP2 c.4364G > T p.R1455I Substitution - Missense ITIH5_ENST00000397146 c.2020C > A p.Q674K Substitution - Missense ITPR2 c.3123 − 1G > A p.? Unknown ITPR2 c.3127G > T p.E1043* Substitution - Nonsense JMJD1C c.5357A > G p.E1786G Substitution - Missense JMJD1C c.5364delA p.E1789fs*45 Deletion - Frameshift JMJD1C_ENST00000399262 c.6068A > G p.E2023G Substitution - Missense JMJD1C_ENST00000399262 c.6075delA p.E2026fs*45 Deletion - Frameshift KCNC1 c.1362_1363insA p.K458fs*16 Insertion - Frameshift KCNC1 c.1363delA p.K457fs*20 Deletion - Frameshift KCNC1_ENST00000265969 c.1362_1363insA p.K458fs*16 Insertion - Frameshift KCNC1_ENST00000265969 c.1363delA p.K457fs*20 Deletion - Frameshift KCNQ1 c.1257G > T p.K419N Substitution - Missense KCNQ1 c.1258delA p.K422fs*10 Deletion - Frameshift KDM2B_ENST00000377071 c.75A > C p.K25N Substitution - Missense KDM2B_ENST00000377071 c.77delA p.K26fs*81 Deletion - Frameshift KDM2B_ENST00000377071 c.82_83delAC p.T28fs*8 Deletion - Frameshift KDM4D c.271delA p.K93fs*4 Deletion - Frameshift KIAA1279 c.1509delA p.I506fs*1 Deletion - Frameshift KIAA1731 c.1649G > A p.R550K Substitution - Missense KIAA1731_ENST00000325212 c.1649G > A p.R550K Substitution - Missense KIAA2018 c.3045A > C p.K1015N Substitution - Missense KIAA2018 c.3046_3047delAA p.N1016fs*8 Deletion - Frameshift KIAA2018 c.3046_3047insA p.N1016fs*9 Insertion - Frameshift KIAA2018 c.3046A > C p.N1016H Substitution - Missense KIAA2018 c.3047delA p.N1016fs*23 Deletion - Frameshift KIAA2026_ENST00000399933 c.2069delA p.K690fs*3 Deletion - Frameshift KIAA2026_ENST00000399933 c.2074T > C p.L692L Substitution - coding silent KIF5B c.1045G > T p.E349* Substitution - Nonsense KIF6 c.1458G > C p.K486N Substitution - Missense KIF6_ENST00000287152 c.1458G > C p.K486N Substitution - Missense KRCC1 c.715A > G p.K239E Substitution - Missense LAMB4 c.4803A > T p.K1601N Substitution - Missense LMOD2_ENST00000458573 c.1432A > C p.K478Q Substitution - Missense LMOD2_ENST00000458573 c.1437G > T p.K479N Substitution - Missense LRRC17 c.597A > C p.K199N Substitution - Missense LRRIQ1 c.818A > G p.E273G Substitution - Missense LRRIQ1_ENST00000393217 c.4615_4616insA p.I1542fs*8 Insertion - Frameshift LRRIQ1_ENST00000393217 c.4616delA p.I1542fs*17 Deletion - Frameshift LRRIQ1_ENST00000393217 c.4623A > G p.K1541K Substitution - coding silent LRRIQ1_ENST00000393217 c.4624A > G p.I1542V Substitution - Missense LRRIQ1_ENST00000393217 c.4625T > A p.I1542N Substitution - Missense LRRIQ1_ENST00000393217 c.5095_5096insA p.N1702fs*13 Insertion - Frameshift LRRIQ1_ENST00000393217 c.5096delA p.N1702fs*20 Deletion - Frameshift LTN1 c.1597_1598delAA p.N536fs*2 Deletion - Frameshift LTN1 c.1607delA p.N536fs*33 Deletion - Frameshift LTN1 c.1608T > G p.N536K Substitution - Missense MAP7D3 c.2567A > C p.K856T Substitution - Missense MAP9 c.1733A > C p.K578T Substitution - Missense MARCKS c.454delA p.K155fs*12 Deletion - Frameshift MCF2 c.773T > A p.I258K Substitution - Missense MCF2 c.774A > T p.I258I Substitution - coding silent MCF2 c.780_781insA p.L261fs*6 Insertion - Frameshift MCF2_ENST00000370573 c.773T > A p.I258K Substitution - Missense MCF2_ENST00000370573 c.774A > T p.I258I Substitution - coding silent MCF2_ENST00000370573 c.780_781insA p.L261fs*6 Insertion - Frameshift MCF2_ENST00000370578 c.1208T > A p.I403K Substitution - Missense MCF2_ENST00000519895 c.953T > A p.I318K Substitution - Missense MCF2_ENST00000519895 c.954A > T p.I318I Substitution - coding silent MCF2_ENST00000519895 c.960_961insA p.L321fs*6 Insertion - Frameshift MIS18BP1 c.471delA p.K157fs*24 Deletion - Frameshift MLH3 c.1755_1756insA p.E586fs*3 Insertion - Frameshift MLH3 c.1755delA p.E586fs*24 Deletion - Frameshift MLH3 c.1756G > T p.E586* Substitution - Nonsense MLH3_ENST00000355774 c.1755_1756insA p.E586fs*3 Insertion - Frameshift MLH3_ENST00000355774 c.1755delA p.E586fs*24 Deletion - Frameshift MLH3_ENST00000355774 c.1756G > T p.E586* Substitution - Nonsense MORC1 c.2634A > C p.E878D Substitution - Missense MORC1 c.2641_2642insA p.I881fs*11 Insertion - Frameshift MORC1 c.2641delA p.I881fs*1 Deletion - Frameshift MPP3 c.1538C > T p.T513M Substitution - Missense MPP6 c.910delA p.K306fs*4 Deletion - Frameshift MTDH c.1341G > A p.K447K Substitution - coding silent MTDH c.1342A > T p.K448* Substitution - Nonsense MTIF2 c.1975T > A p.F659I Substitution - Missense MYCBP2 c.1124delA p.K375fs*4 Deletion - Frameshift MYCBP2_ENST00000357337 c.1124delA p.K375fs*4 Deletion - Frameshift MYCBP2_ENST00000407578 c.1238delA p.K413fs*4 Deletion - Frameshift MYT1L c.182G > T p.R61I Substitution - Missense MYT1L c.187A > G p.T63A Substitution - Missense NAA16 c.1883G > C p.R628T Substitution - Missense NAA35 c.1692G > A p.K564K Substitution - coding silent NAA35 c.1693delA p.K567fs*6 Deletion - Frameshift NEK1 c.3156A > G p.K1052K Substitution - coding silent NEK1_ENST00000507142 c.3156A > G p.K1052K Substitution - coding silent NHLRC2 c.1517_1518insA p.N508fs*13 Insertion - Frameshift NHLRC2 c.1522A > C p.N508H Substitution - Missense NIPBL c.1507delA p.R505fs*35 Deletion - Frameshift NIPBL_ENST00000448238 c.1507delA p.R505fs*35 Deletion - Frameshift NKRF c.700A > C p.K234Q Substitution - Missense NKRF_ENST00000542113 c.745A > C p.K249Q Substitution - Missense NKTR c.1297_1298insA p.V436fs*2 Insertion - Frameshift NOL7 c.707delA p.K238fs*16 Deletion - Frameshift NOL7 c.716delA p.N240fs*14 Deletion - Frameshift NOP58 c.1564delA p.K524fs* > 6 Deletion - Frameshift NUFIP1 c.494delA p.K165fs*38 Deletion - Frameshift NUP85 c.127 + 2T > C p.? Unknown OR6C76 c.921_922insA p.H312fs* > 2 Insertion - Frameshift OR6C76 c.921C > A p.H307Q Substitution - Missense OR6C76 c.922_923delAA p.K311fs* > 2 Deletion - Frameshift OR6C76 c.922delA p.K311fs* > 2 Deletion - Frameshift OR6C76 c.932A > C p.K311T Substitution - Missense PA2G4 c.1108delA p.K372fs*16 Deletion - Frameshift PA2G4 c.1116G > T p.K372N Substitution - Missense PARP14 c.4200G > T p.K1400N Substitution - Missense PARP14_ENST00000474629 c.4689G > T p.K1563N Substitution - Missense PCDH7 c.2685A > G p.K895K Substitution - coding silent PCDH7_ENST00000361762 c.2826A > G p.K942K Substitution - coding silent PCDHA12 c.552delA p.D187fs*8 Deletion - Frameshift PCDHA12 c.559G > T p.D187Y Substitution - Missense PDCL2 c.253A > G p.K85E Substitution - Missense PDCL2 c.262A > C p.K88Q Substitution - Missense PKD2L2 c.904delA p.I304fs*1 Deletion - Frameshift PKD2L2 c.916G > T p.E306* Substitution - Nonsense PKD2L2_ENST00000508883 c.916G > T p.E306* Substitution - Nonsense PLXNC1 c.4192delA p.I1400fs*21 Deletion - Frameshift PLXNC1 c.4196A > C p.K1399T Substitution - Missense PNISR c.806A > G p.K269R Substitution - Missense PNISR c.807_808insA p.A270fs*6 Insertion - Frameshift PPFIA2 c.2527A > G p.K843E Substitution - Missense PPFIA2 c.2529A > G p.K843K Substitution - coding silent PPP1R10 c.924A > G p.K308K Substitution - coding silent PPP1R10 c.930delA p.V311fs*79 Deletion - Frameshift PPP2R3C c.67_68insA p.S23fs*2 Insertion - Frameshift PPP2R3C c.67delA p.S23fs*5 Deletion - Frameshift PRKDC c.10814delA p.N3605fs*48 Deletion - Frameshift PRKDC c.496_497insA p.I166fs*11 Insertion - Frameshift PRKDC c.496delA p.I166fs*6 Deletion - Frameshift PRPF40A c.1167 + 3A > T p.? Unknown PRPF40A_ENST00000359961 c.1560 + 3A > T p.? Unknown PRPF40A_ENST00000410080 c.1479 + 3A > T p.? Unknown PRR11 c.58delA p.E23fs*9 Deletion - Frameshift PTHLH_ENST00000354417 c.557delA p.K186fs*12 Deletion - Frameshift PTPLAD1 c.1074G > T p.K358N Substitution - Missense PTPLAD1 c.1077A > C p.K359N Substitution - Missense PTPRC c.2404G > T p.E802* Substitution - Nonsense PTPRZ1 c.5636delA p.K1879fs*34 Deletion - Frameshift PTPRZ1_ENST00000393386 c.5636delA p.K1879fs*34 Deletion - Frameshift PXK c.1367_1368insA p.R459fs*15 Insertion - Frameshift PXK_ENST00000356151 c.1367_1368insA p.R459fs*15 Insertion - Frameshift PYHIN1 c.416_417insA p.P142fs*3 Insertion - Frameshift PYHIN1 c.423_424insA p.P142fs*3 Insertion - Frameshift PYHIN1 c.424C > A p.P142T Substitution - Missense PYHIN1_ENST00000368135 c.424C > A p.P142T Substitution - Missense PYH1N1_ENST00000392254 c.424C > A p.P142T Substitution - Missense Q99543-2 c.590_591insA p.N197fs*4 Insertion - Frameshift Q99543-2 c.590delA p.N197fs*8 Deletion - Frameshift RAD23B_ENST00000457811 c.312_313delAA p.K108fs*38 Deletion - Frameshift RALGAPA1 c.5582delA p.N1861fs*6 Deletion - Frameshift RALGAPA1_ENST00000307138 c.5582delA p.N1861fs*6 Deletion - Frameshift RASAL2 c.1097A > G p.E366G Substitution - Missense RASAL2 c.1104_1105insA p.D372fs*4 Insertion - Frameshift RASAL2 c.1104G > C p.K368N Substitution - Missense RASAL2 c.1105_1106insA p.D372fs*4 Insertion - Frameshift RASAL2 c.1105delA p.K371fs*7 Deletion - Frameshift RASAL2 c.1111_1112insA p.D372fs*4 Insertion - Frameshift RASAL2 c.1112_1113insA p.D372fs*4 Insertion - Frameshift RASAL2_ENST00000367649 c.1151A > G p.E384G Substitution - Missense RASAL2_ENST00000367649 c.1158_1159insA p.D390fs*4 Insertion - Frameshift RASAL2_ENST00000367649 c.1158G > C p.K386N Substitution - Missense RASAL2_ENST00000367649 c.1159_1160insA p.D390fs*4 Insertion - Frameshift RASAL2_ENST00000367649 c.1159delA p.K389fs*7 Deletion - Frameshift RASAL2_ENST00000367649 c.1165_1166insA p.D390fs*4 Insertion - Frameshift RASAL2_ENST00000367649 c.1166_1167insA p.D390fs*4 Insertion - Frameshift RASAL2_ENST00000462775 c.707A > G p.E236G Substitution - Missense RASAL2_ENST00000462775 c.714_715insA p.D242fs*4 Insertion - Frameshift RASAL2_ENST00000462775 c.714G > C p.K238N Substitution - Missense RASAL2_ENST00000462775 c.715_716insA p.D242fs*4 Insertion - Frameshift RASAL2_ENST00000462775 c.715delA p.K241fs*7 Deletion - Frameshift RBM43 c.205G > T p.E69* Substitution - Nonsense RBM43 c.213_214insA p.V72fs*18 Insertion - Frameshift RBM43 c.213delA p.V72fs*13 Deletion - Frameshift RBMX2 c.491delA p.K166fs*29 Deletion - Frameshift RBMX2 c.498_499insA p.K170fs*30 Insertion - Frameshift RBMX2 c.503A > C p.K168T Substitution - Missense RBMX2 c.505A > G p.K169E Substitution - Missense RBMX2 c.506A > G p.K169R Substitution - Missense RBMX2 c.511_514delGAAA p.E171fs*23 Deletion - Frameshift RBPJ c.202delA p.E71fs*21 Deletion - Frameshift RBPJ c.204A > G p.K68K Substitution - coding silent RBPJ_ENST00000348160 c.205delA p.E72fs*21 Deletion - Frameshift RBPJ_ENST00000348160 c.207A > G p.K69K Substitution - coding silent RDX c.628A > C p.N210H Substitution - Missense REV3L c.4543G > A p.E1515K Substitution - Missense REV3L c.4543G > T p.E1515* Substitution - Nonsense REV3L c.4550T > C p.I1517T Substitution - Missense REV3L_ENST00000358835 c.4777G > T p.E1593* Substitution - Nonsense REV3L_ENST00000358835 c.4784T > C p.I1595T Substitution - Missense RG9MTD1 c.384delA p.K131fs*3 Deletion - Frameshift RIF1 c.4507delA p.K1505fs*18 Deletion - Frameshift RNASEH2B c.917A > C p.K306T Substitution - Missense RNASEH2B c.926T > A p.I309N Substitution - Missense RNASEH2B c.926T > C p.I309T Substitution - Missense RNF145 c.68A > G p.K23R Substitution - Missense RNF145 c.68delA p.K23fs*17 Deletion - Frameshift RNF145 c.69G > A p.K23K Substitution - coding silent RNF145 c.70A > G p.K24E Substitution - Missense RNF145 c.71A > G p.K24R Substitution - Missense RNF145 c.79_80delAA p.N27fs*43 Deletion - Frameshift RNF145 c.80delA p.N27fs*13 Deletion - Frameshift RNF145 c.81C > A p.N27K Substitution - Missense RNPC3 c.346_347insA p.R120fs*3 Insertion - Frameshift RNPC3 c.347delA p.R120fs*18 Deletion - Frameshift ROCK1_ENST00000399799 c.149A > C p.K50T Substitution - Missense RPL9 c.150G > A p.K50K Substitution - coding silent RPL9 c.158A > G p.K53R Substitution - Missense RPL9 c.159G > T p.K53N Substitution - Missense RSPO3 c.659_660insA p.P223fs*2 Insertion - Frameshift RYR1 c.8508G > T p.K2836N Substitution - Missense RYR1 c.8509delA p.T2839fs*89 Deletion - Frameshift SAT1_ENST00000379251 c.439delA p.N150fs*13 Deletion - Frameshift SCAF11 c.2995_2999delGAAAA p.E999fs*2 Deletion - Frameshift SCAF11 c.3002_3003insA p.N1001fs*2 Insertion - Frameshift SCAF11 c.3002delA p.N1001fs*5 Deletion - Frameshift SCAPER c.2603delA p.N868fs*8 Deletion - Frameshift SCAPER c.2605A > T p.K869* Substitution - Nonsense SCAPER c.2613delA p.A872fs*4 Deletion - Frameshift SCAPER_ENST00000538941 c.1867A > T p.K623* Substitution - Nonsense SCAPER_ENST00000538941 c.1875delA p.A626fs*4 Deletion - Frameshift SEC63 c.1586delA p.K529fs*4 Deletion - Frameshift SEC63 c.1587G > T p.K529N Substitution - Missense SENP7 c.230A > G p.K77R Substitution - Missense SENP7_ENST00000394095 c.230A > G p.K77R Substitution - Missense SEPT7_ENST00000469679 c.683C > A p.A228E Substitution - Missense SH3RF1 c.2151G > A p.K717K Substitution - coding silent SHPRH c.495_496insA p.E166fs*7 Insertion - Frameshift SHPRH c.495delA p.E166fs*3 Deletion - Frameshift SLC16A12_ENST00000371790 c.83G > C p.R28T Substitution - Missense SLC22A9 c.1005A > C p.K335N Substitution - Missense SLC22A9 c.995delA p.K335fs*67 Deletion - Frameshift SLC45A2 c.865A > C p.K289Q Substitution - Missense SLC46A3 c.154A > C p.K52Q Substitution - Missense SLC46A3_ENST00000380814 c.154A > C p.K52Q Substitution - Missense SLC4A7 c.3450G > C p.K1150N Substitution - Missense SLCO5A1 c.1148A > G p.K383R Substitution - Missense SLCO5A1 c.1150T > G p.F384V Substitution - Missense SLTM c.1539delA p.E514fs*8 Deletion - Frameshift SLTM c.1540G > T p.E514* Substitution - Nonsense SMAD5 c.137A > G p.K46R Substitution - Missense SMC1B_ENST00000357450 c.2444C > G p.T815S Substitution - Missense SMC2 c.814delA p.I274fs*1 Deletion - Frameshift SMC2 c.822A > G p.I274M Substitution - Missense SMC2_ENST00000303219 c.822A > G p.I274M Substitution - Missense SMC2L1 c.814delA p.I274fs*1 Deletion - Frameshift SMC2L1 c.822A > G p.I274M Substitution - Missense SMNDC1 c.567C > A p.N189K Substitution - Missense SNX6 c.538A > T p.K180* Substitution - Nonsense SP100_ENST00000341950 c.1349_1350insA p.K455fs* > 20 Insertion - Frameshift SPATA1 c.1345delA p.I452fs*1 Deletion - Frameshift SPEF2 c.711G > A p.K237K Substitution - coding silent SPEF2 c.712A > G p.K238E Substitution - Missense SPEF2_ENST00000356031 c.2649_2650delAA p.K886fs*2 Deletion - Frameshift SPEF2_ENST00000356031 c.2649delA p.K886fs*8 Deletion - Frameshift SPEF2_ENST00000356031 c.711G > A p.K237K Substitution - coding silent SPEF2_ENST00000356031 c.712A > G p.K238E Substitution - Missense SPINK5 c.2459delA p.K823fs*101 Deletion - Frameshift SREK1IP1 c.363A > C p.K121N Substitution - Missense SYCP1 c.2891_2892insA p.L968fs*5 Insertion - Frameshift SYCP1 c.2892delA p.K967fs*2 Deletion - Frameshift SYCP2 c.3062_3063insT p.N1024fs*3 Insertion - Frameshift SYCP2 c.3071delA p.N1024fs*26 Deletion - Frameshift TAF1B c.187_188delAA p.N66fs*3 Deletion - Frameshift TAF1B c.187_189delAAA p.K65delK Deletion - In frame TAF1B c.187delA p.N66fs*26 Deletion - Frameshift TAF1B c.198C > A p.N66K Substitution - Missense TAF1D c.281_282insA p.K95fs*28 Insertion - Frameshift TAF1D c.281delA p.K94fs*26 Deletion - Frameshift TAF7L c.1331A > C p.Q444P Substitution - Missense TAF7L c.1333A > C p.K445Q Substitution - Missense TAOK1_ENST00000261716 c.1738G > A p.E580K Substitution - Missense TCF25 c.384_385insA p.Q132fs*27 Insertion - Frameshift TCF25 c.385delA p.K131fs*17 Deletion - Frameshift TCF25 c.393_394insA p.Q132fs*27 Insertion - Frameshift TCOF1 c.4127delA p.E1379fs* > 33 Deletion - Frameshift TCOF1_ENST00000504761 c.4358delA p.E1456fs* > 33 Deletion - Frameshift TCP1 c.730A > C p.T244P Substitution - Missense TDRD5 c.1243G > A p.E415K Substitution - Missense TET1_ENST00000373644 c.57C > A p.N19K Substitution - Missense TETl_ENST00000373644 c.58delA p.K22fs*23 Deletion - Frameshift TEX10 c.11_13delAAA p.K4delK Deletion - In frame TEX10 c.13delA p.R5fs*10 Deletion - Frameshift TEX15 c.5122delA p.R1708fs*3 Deletion - Frameshift TFAM c.432delA p.E148fs*2 Deletion - Frameshift TFAM c.441 + 2T > G p.? Unknown TFAM_ENST00000395377 c.376delA p.T126fs*6 Deletion - Frameshift THOC2 c.2531A > G p.K844R Substitution - Missense THOC2_ENST00000245838 c.2768A > G p.K923R Substitution - Missense TIF1 c.2574G > A p.K858K Substitution - coding silent TMEM97 c.518_519insA p.*177fs? Insertion - Frameshift TMEM97 c.519delA p.K176fs? Deletion - Frameshift TNRC6A c.104A > C p.K35T Substitution - Missense TNRC6B_ENST00000301923 c.179A > G p.K60R Substitution - Missense TNRC6B_ENST00000301923 c.180G > A p.K60K Substitution - coding silent TNRC6B_ENST00000301923 c.182A > C p.K61T Substitution - Missense TNRC6B_ENST00000454349 c.113A > G p.K38R Substitution - Missense TNRC6B_ENST00000454349 c.114G > A p.K38K Substitution - coding silent TNRC6B_ENST00000454349 c.116A > C p.K39T Substitution - Missense TPR c.2055A > C p.E685D Substitution - Missense TPR c.2056A > T p.K686* Substitution - Nonsense TRDN c.1145A > G p.K382R Substitution - Missense TRIM24 c.2676G > A p.K892K Substitution - coding silent TRIM59 c.594G > T p.Q198H Substitution - Missense TRIM59 c.604delA p.S202fs*3 Deletion - Frameshift TRMT6 c.458delA p.K153fs*9 Deletion - Frameshift TRPC1 c.509A > G p.K170R Substitution - Missense TTF1 c.1007_1008insA p.K337fs*9 Insertion - Frameshift TTF1 c.1007delA p.K336fs*87 Deletion - Frameshift TWISTNB c.932_933insA p.K312fs*6 Insertion - Frameshift TWISTNB c.932delA p.K311fs*15 Deletion - Frameshift TWISTNB c.933G > T p.K311N Substitution - Missense TWISTNB c.935_936insG p.R313fs*5 Insertion - Frameshift TWISTNB c.938G > A p.R313K Substitution - Missense ULK4_ENST00000301831 c.1778delA p.K593fs*17 Deletion - Frameshift USP36 c.2874_2879delGAAAAA p.K959_K960delKK Deletion - In frame USP36_ENST00000312010 c.2874_2879delGAAAAA p.K959_K960delKK Deletion - In frame USP36_ENST00000312010 c.2874G > A p.K958K Substitution - coding silent USP40 c.3468G > T p.K1156N Substitution - Missense USP40 c.3477_3478insA p.Q1160fs*20 Insertion - Frameshift USP40 c.3477delA p.K1159fs*12 Deletion - Frameshift USP40_ENST00000450966 c.3468G > T p.K1156N Substitution - Missense USP40_ENST00000450966 c.3477_3478insA p.Q1160fs*20 Insertion - Frameshift USP40_ENST00000450966 c.3477delA p.K1159fs*12 Deletion - Frameshift VAX1 c.473A > C p.K158T Substitution - Missense VAX1 c.477A > G p.K159K Substitution - coding silent VAX1 c.477delA p.K159fs* > 28 Deletion - Frameshift VAX1 c.478C > G p.Q160E Substitution - Missense VAX1 c.480A > C p.Q160H Substitution - Missense VAX1 c.483G > T p.K161N Substitution - Missense WDHD1 c.1827G > A p.K609K Substitution - coding silent WNK1 c.1738_1749ins? p.? Unknown WNK1 c.1739delA p.K583fs*11 Deletion - Frameshift WNK1 c.1740A > G p.E580E Substitution - coding silent WNK1 c.1749G > T p.K583N Substitution - Missense WNK1_ENST00000537687 c.1739delA p.K583fs*11 Deletion - Frameshift WNK1_ENST00000537687 c.1740A > G p.E580E Substitution - coding silent WNK1_ENST00000537687 c.1749G > T p.K583N Substitution - Missense ZC3H13 c.3719G > C p.S1240T Substitution - Missense ZC3H13 c.3719G > T p.S1240I Substitution - Missense ZCCHC9 c.189G > T p.K63N Substitution - Missense ZCCHC9 c.196G > T p.E66* Substitution - Nonsense ZCRB1 c.411G > A p.K137K Substitution - coding silent ZCRB1 c.419_420insA p.K141fs*4 Insertion - Frameshift ZCRB1 c.419delA p.K140fs*13 Deletion - Frameshift ZFHX3 c.1031A > T p.N344I Substitution - Missense ZFR c.1074_1075insA p.E359fs*27 Insertion - Frameshift ZFR c.1074delA p.E359fs*4 Deletion - Frameshift ZMAT1 c.1276A > T p.K426* Substitution - Nonsense ZMAT1 c.1277A > T p.K426I Substitution - Missense ZMAT1 c.1278A > G p.K426K Substitution - coding silent ZMAT1_ENST00000372782 c.1789A > T p.K597* Substitution - Nonsense ZMAT1_ENST00000372782 c.1790A > T p.K597I Substitution - Missense ZMAT1_ENST00000372782 c.1791A > G p.K597K Substitution - coding silent ZMYM5_ENST00000337963 c.1934delA p.N645fs* > 25 Deletion - Frameshift ZNF236 c.1373delA p.M461fs*1 Deletion - Frameshift ZNF236_ENST00000543926 c.1373delA p.M461fs*1 Deletion - Frameshift ZNF34 c.664delA p.T222fs*15 Deletion - Frameshift ZNF518A c.2777delA p.T929fs*2 Deletion - Frameshift ZNF518A_ENST00000371192 c.2777delA p.T929fs*2 Deletion - Frameshift ZNF600 c.194_195insA p.L66fs*4 Insertion - Frameshift ZNF644 c.871delA p.R291fs*7 Deletion - Frameshift ZNF644 c.872G > T p.R291I Substitution - Missense

Materials and Methods for Example 1 CELL CULTURE

HDF cells were cultured in Dulbecco's modified Eagle's medium (Gibco) and supplemented with 10% fetal bovine serum, 5% MEM non-essential amino acids (100×, Gibco), 5% penicillin and streptomycin (Gibco), and L-glutamine (Gibco). T-Rex-CHO cells were grown in Ham's F12K medium (ATCC) with the same supplements. Drosophila S2 cells were cultured in Express Five SFM Medium (Invitrogen) supplemented with 100 units per milliliter penicillin, 100 units per milliliter streptomycin (Gibco) and 45 ml of 200 mM L-glutamine (Gibco) per 500 ml of medium.

Plasmids and mRNA were introduced to the cells by the Neon® Transfection System (Invitrogen) with 100 μl tips according to cell specific protocols (www.lifetechnologies.com/us/en/home/life-science/cell-culture/transfection/transfection-selection-misc/neon-transfection-system/neon-protocols-cell-line-data.html). Cells electroporated with DNA plasmids were harvested after 48 hours if not indicated differently. Cells electroporated with mRNA were harvested after 4 hours, if not indicated differently. All transfections in S2 cells were performed using Effectene reagent (Qiagen).

DNA CONSTRUCTS

mCherry reporter constructs were generated by PCR amplification of an mCherry template with forward primers containing the test sequence at the 5′ end and homology to mCherry at the 3′ end. The test sequence for each construct is listed in Table 5. The PCR product was purified by NucleoSpin Gel and PCR Clean-up kit (Macherey-Nagel) and integrated into the pcDNA-DEST40, pcDNA-DEST53 or pMT-DEST49 expression vector by the Gateway cloning system (Invitrogen). Luciferase constructs were generated by the same method.

Whole gene constructs were generated by PCR amplification from gene library database constructs from Thermo (MTDH CloneId:5298467) or Life Technologies GeneArt Strings DNA Framents (ZCRB1) and cloned in pcDNA-DEST40 vector for expression. Synonymous mutations in the natural gene homopolymeric lysine runs were made by site directed mutagenesis. Human beta-globin gene (HBD, delta chain) was amplified from genomic DNA isolated from HDF cells. Insertions of poly(A)-track, AAG-codons or pre-mature stop codon in HBD constructs were made by site directed mutagenesis. Sequences of inserts are in the Table 5.

TABLE 5 Sequences of mCherry inserts Sequence inserted between SEQ 2HA tag and ID Construct mCherry NO: WT No sequence inserted GAA₁₂ GAA GAA GAA GAA GAA GAA GAA GAA 1 GAA GAA GAA GAA AAG₆ AAG AAG AAG AAG AAG AAG 2 AAG₉ AAG AAG AAG AAG AAG AAG AAG AAG 3 AAG AAG₁₂ AAG AAG AAG AAG AAG AAG AAG AAG 4 AAG AAG AAG AAG STOP TAA AAA₆ AAA AAA AAA AAA AAA AAA 5 AAA₉ AAA AAA AAA AAA AAA AAA AAA AAA AAA 6 AAA₁₂ AAA AAA AAA AAA AAA AAA AAA AAA AAA 7 AAA AAA AAA CGA₁₂ CGA CGA CGA CGA CGA CGA CGA CGA 8 CGA CGA CGA CGA AGG₁₂ AGG AGG AGG AGG AGG AGG AGG AGG 9 AGG AGG AGG AGG A9 GCA GCG AAA AAA AAA TCC GTG 10 A10 GCA AAA AAA AAA GTG 11 A11 GCA GCA AAA AAA AAA ACC GTG 12 A12 GCA GAA AAA AAA AAA ACC GTG 13 A13 GCA GAA AAA AAA AAA AAC GTG 14 SLU7 GAG AAG AAG AAG AAG AAA AAG AAG 15 AAG AAG AAG CAT MTDH TCC AAA AAG AAA AAA AAG AAA AAG 16 AAG AAG CAA GGT Nop58 GAG AAA AAG AAG AAA AAG AAA AAA 17 AAG AGA GAG AGA ZCRB1 CCA AAG AAG AAA GAA AAA AAG AAA 18 AAA AAG AAA GCT RASAL2 GTG GAA AAA AAG AAA AAA AAG GAC 19 AAG AAT AAT TAT ZCRB1 CCA AAG AAG AAA GAA AAA AAG AAA 20 AAA AAG AAA GCT ZCRB1 G > A CCA AAG AAG AAA GAA AAA AAA AAA 21 AAA AAG AAA GCT ZCRB1 A > G CCA AAG AAG AAA GAA AAG AAG AAA 22 AAG AAG AAA GCT RASAL2 GTG GAA AAA AAG AAA AAA AAG GAC 23 AAG AAT AAT TAT RASAL2 GTG GAA AAA AAA AAA AAA AAG GAC 24 G > A AAG AAT AAT TAT RASAL2 GTG GAA AAA AAG AAA AAG AAG GAC 25 A > G AAG AAT AAT TAT RASAL2 GTG GAA AAG AAG AAG AAG AAG GAC 26 A > G(3) AAG AAT AAT TAT

IN VITRO MRNA SYNTHESIS

Capped and polyadenylated mRNA was synthesized in vitro using m Message mMachine T7 Transcription Kit (LifeTechnologies) following manufacturers procedures. The quality of mRNA was checked by electrophoresis and sequencing of RT-PCR products.

RNA EXTRACTION AND QRT-PCR

Total RNA was extracted from cells using the Ribozol RNA extraction reagent (Amresco) according to the manufacturer's instructions. 400 μl of Ribozol reagent was used per well of 6 or 12 well plates for RNA extraction. Precipitated nucleic acids were treated by Turbo DNAse (Ambion) and total RNA was dissolved in RNAse-free water and stored at −20° C. RNA concentration was measured by Nanodrop (0D260/280). iScript Reverse Transcription Supermix (Biorad) was used with 1 μg of total RNA following the manufacturer's protocol. iQ SYBR Green Supermix (Biorad) protocol was used for qRT-PCR on the CFX96 Real-Time system with Bio-Rad CFX Manager 3.0 software. Cycle threshold (Ct) values were normalized to the neomycin resistance gene expressed from the same plasmid.

WESTERN BLOT ANALYSIS

Total cell lysates were prepared with passive lysis buffer (Promega). Blots were blocked with 5% milk in 1×TBS 0.1% Tween-20 (TBST) for 1 hour. HRP-conjugated or primary antibodies were diluted by manufacturer recommendations and incubated overnight with membranes. Membranes were washed 4 times for 5 minutes in TBST and prepared for imaging or secondary antibody was added for additional one hour incubation. Images were generated by Bio-Rad Molecular Imager ChemiDoc XRS System with Image Lab software by chemiluminescence detection or by the LI-COR Odyssey Infrared Imaging System. Blots imaged by the LI-COR system were first incubated for 1 hr with Pierce DyLight secondary antibodies.

Immunoprecipitation

Total cell lysates were prepared with passive lysis buffer (Promega) and incubated with Pierce anti-HA magnetic beads overnight at 4° C. Proteins were eluted by boiling the beads with 1× SDS sample buffer for 7 minutes. Loading of protein samples was normalized to total protein amounts.

Cell Imaging

HDF cells were electroporated with the same amount of DNA plasmids and plated in 6 well plates with the optically clear bottom. Prior to imaging, cells were washed with a fresh DMEM media without Phenol-Red and incubated 20 minutes with DMEM media containing 0.025% Hoechst 33342 dye for DNA staining. Cells were washed with DMEM media and imaged in Phenol-Red free media using an EVOS-FL microscope (40× objective). Images were analyzed using EVOS-FL software.

Sequence data and variation databases: Sequence data were derived from NCBI RefSeq resource (Pruitt et al. (2014) RefSeq: an update on mammalian reference sequences. Nucleic Acids Res. 42, D756-763), on February 2014. Two variations databases were used: dbSNP (Sherry et al. (2001) Nucleic Acids Res. 29, 308-311), build 139 and COSMIC, build v70 (Forbes et al. (2014) Nucleic Acids Res.).

mRNA MAPPING

As some inconsistences between transcripts and proteins were observed in some of the sequence databases, before starting the analyses protein sequences were mapped to mRNA sequences using exonerate tool (Slater & Birney (2005) BMC Bioinformatics 6, 31), using protein2genome model and requiring a single best match. In case of multiple best matches (when several transcripts had given identical results), a first one was chosen, as the choice of corresponding isoform (as this was the most common reason for multiple matches) did not influence downstream analyses.

RIBOSOME PROFILING DATA

Three independent studies of ribosome profiling data from human cells were analyzed. These were: GSE51424 prepared by Gonzales and coworkers (Gonzalez et al. (2014) J. Neurosci. Off. J. Soc. Neurosci. 34, 10924-10936) from which samples: SRR1562539, SRR1562540 and SRR1562541 were used; GSE48933 prepared by Rooijers and coworkers (Rooijers et al. (2013) Nat. Commun. 4) from which samples: SRR935448, SRR935449, SRR935452, SRR935453, SRR935454 and SRR935455 were used; GSE42509 prepared by Loayza-Puch and coworkers (Loayza-Puch et al. (2013) Genome Biol. 14, R32) from which samples SRR627620-SRR627627 were used. The data were analyzed similarly to the original protocol created by Ingolia and coworkers (Ingolia et al. (2012) Nat. Protoc. 7, 1534-1550), with modifications reflecting the fact that reads were mapped to RNA data, instead of genome.

Raw data were downloaded and adapters specific for each experiments were trimmed. Then the reads were mapped to human noncoding RNAs with bowtie 1.0.1 (Langmead et al. (2009) Genome Biol. 10, R25) (bowtie-p 12-t-un) and unaligned reads were mapped to human RNAs (bowtie-p 12-v 0-a-m 25-best-strata-suppress 1,6,7,8). The analysis of occupancy was originally done in a similar way to Charneski and Hurst ((2013) PLoS Biol. 11, e100150817), however, given that genes with polyA were not highly expressed and the data were sparse (several positions with no occupancy), instead of mean of 30 codons prior to polyA position, it was decided to normalize only against occupancy of codon at the position 0 multiplied by the average occupancy along the gene. Occupancy data were visualized with R and Ggplot2 library using geom_boxplot aesthetics. On all occupancy graphs, the upper and lower “hinges” correspond to the first and third quartiles (the 25th and 75th percentiles). The upper and lower whiskers extend from hinges at 1.5*IQR of the respective hinge.

VARIATION ANALYSIS

To assess the differences in SNPs in polyA regions vs random region of the same length in other genes, the same distribution of lengths in both cases needed to be used. The distribution of lengths for polyA regions identified as mentioned above (12 As allowing for one mismatch) up to length 19 (longer are rare) is presented in FIG. 27 . Using the same distribution of lengths, one random region of length drawn from the distribution randomly placed along each gene from all human protein coding RNAs was selected. Distributions of number of SNPs per segment for all polyA segments and for one random segment for each mRNA were compared using Welch Two Sample t-test, Wilcoxon rank sum test with continuity correction and two sample permutation test with 100000 permutations.

ABUNDANCE OF POLYTRACKS IN PROTEIN SEQUENCES

Abundance was expressed by a following equation:

${Abundance}{= \frac{1}{{- \log_{10}}\frac{N_{P}}{N_{R}}}}$

where NP is number of proteins with K+ polytrack (at least 2, at least 3, etc.) and NR is the total number of occurrences of a particular amino acid. It is to normalize against variable amino acid presence in different organisms. All isoforms of proteins were taken into account.

OTHER ANALYSES

List of human essential genes was obtained from the work of Georgi and coworkers (PLoS Genet 9, e1003484 (2013)). Gene Ontology analyses were done using Term Enrichment Service at amigo.geneontology.org/rte. Most of graphs were prepared using the R and GGPLOT2 library. For FIG. 14A, the values of the Y-axis were computed by 1D gaussian kernel density estimates implemented in R software. Custom Perl scripts were used to analyze and merge the data.

EXAMPLE 2: PolyA Tracks can be Used to Regulate Gene Expression in Escherichia Coli

We have recently identified polyA tracks as a regulator of gene expression. This mechanism is used endogenously in most eukaryotic genomes and regulates approximately 2% of human genes (Arthur, et al., 2015; Habich, et al., 2016). The polyA track causes ribosomal stalling and frameshifting during translation elongation, leading to mRNA instability and degradation of nascent protein products (Arthur, et al., 2015; Koutmou, et al., 2015). The translation elongation cycle is an ideal target for a universal method of gene regulation because it is the most highly conserved step in protein biosynthesis between prokaryotes and eukaryotes (Melnikov, et al., 2012). We have thus reasoned that polyA tracks, due to their versatility in lengths and sequence composition, can be used as a system to create programmable hypomorphic mutants and regulate gene expression in wide variety of model organisms (FIG. 29 ).

We have generated a fluorescent reporter gene that has an insertion of defined polyA tracks in order to control the amount of expression (FIG. 29A). The reporter consists of either a constitutive or inducible promoter driving expression of the mCherry fluorescence and other reporter proteins. A double HA-tag was added at the beginning of the coding sequence for detection on western blot analysis. The polyA track is inserted directly after the HA-tag. The length of the polyA track varies from 9 to 36 consecutive adenine nucleotides, adding 3 to 12 lysine residues to the protein sequence (FIG. 29A). To control for the effects of polybasic peptide arising from sequential lysine residues (Kuroha, et al., 2010; Brandman, et al., 2012), we generated control reporters with consecutive lysine AAG codons. We hypothesized that as the length of the polyA track is increased, expression of the reporter gene products will decrease (FIGS. 29B and 29C). These reporters can be transiently transfected, recombined or inserted into the genome of cell cultures or whole organisms. Likewise, endogenous genes can be edited to include a polyA tracks in their open reading frames (ORF's) using genome editing methodology.

We first tested whether polyA tracks can be used in single cell model organisms to attenuate gene expression from a defined reporter gene. To show that polyA tracks can be used to control gene expression in E. coli cells we created a set of reporters with increasing length of polyA tracks under the arabinose-inducible promoter pBAD (FIG. 31 ). We transformed the chemically competent E. coli cells (Top10 strain) with plasmids expressing HA-mCherry, HA-(AAG)n-mCherry or HA-polyA-mCherry. All E. coli cell cultures were induced at the same optical density and monitored for both cell growth and fluorescence of the mCherry constructs during induction. While E. coli containing wild type and LysAAG controls (6×, 9× and 12× lysine AAG codons) show no significant differences in the amount of mCherry fluorescence, cell cultures containing constructs with polyA tracks show progressively less fluorescence with increasing length of the polyA track (FIG. 26A). Addition of 9 and 12A's in a row (3 or 4 LysAAA codons) consistently reduced fluorescence of mCherry reporter by 15-35%. Further additions in the length of the polyA track resulted in constant decrease of mCherry reporter fluorescence where 36 consecutive adenine nucleotides resulted in a barely visible expression of the reporter (<5% of wild type). Western blot analyses of equal amounts of E. coli cell lysates expressing different polyA track and control reporters confirmed mCherry fluorescence data and indicated again that protein abundances of polyA track reporters strongly depend on the length of polyA track (FIG. 26B). Reporters with 9 and 12As in the row (3 and 4LysAAA codons, respectively) show reduction in protein abundances in the range of 20-40% of the wild type mCherry and constructs with more than 27As in the row (9 and more LysAAA codons) were hardly detectable by western blot analyses.

EXAMPLE 3: PolyA Tracks can be Used to Regulate Gene Expression in Protozoan Tetrahymena Thermophile

We previously showed that polyA tracks can influence expression of the reporter genes in S. cerevisiae (Koutmou, et al., 2015) cells. To test whether polyA tracks can regulate gene expression in another model single cell eukaryotic organism, we monitored the effect of various length tracks on YFP expression in the protozoan T. thermophila. The genome of T. thermophila has extremely high AT content (>75%) and has been extensively used as microbial animal model [Collins, K. and M. A. Gorovsky (2005). “Tetrahymena thermophila.” Curr Biol 15(9): R317-318.] (Eisen, et al., 2006). Our T. thermophila reporter contained the coding sequence of a Macronucleus-Localized Protein of unknown function (MLP1, TTHERM_00384860) fused to eYFP protein (FIG. 45A-D). The fusion with MLP1 directed YFP to Tetrahymena macronuclei to allow easier quantification of YFP levels (FIG. 26C). These two proteins were fused, separated by linkers containing an HA-tag (MLP1-HA-YFP (WT)) and polyA tracks of 18, 27, or 36As, (AAA)6, (AAA)9, or (AAA)12, respectively, or 12 LysAAG (AAG)12 codons inserted as a control. All constructs were expressed upon cadmium-induction of the upstream MTT1 promoter. Just as in our E. coli experiments with mCherry reporter, the YFP gene containing increasing lengths of polyA tracks exhibited a progressive decrease in total protein accumulation, measured by fluorescence, relative to the HA-linker fusion or LysAAG insertion controls (FIG. 26D). The construct with 18As in a row (6LysAAA) showed approximately 50% reduction in protein fluorescence, while constructs with 27 and 36As required 20 times longer exposure for detection of YFP by microscopy. The construct with 12LysAAG codons showed fluorescence that was readily 4-5 fold lower then WT construct. This effect could be attributed to polybasic peptide stalling that was observed earlier in S. cerevisiae cells (Koutmou, et al., 2015; Kuroha, et al., 2010; Brandman, et al., 2012). We further confirmed our fluorescence results by Western blot analyses (FIG. 26E). The MLP1-HA-YFP-fusion (WT) was readily visible whereas the polyA track-YFP fusions showed attenuation of expression. Insertion of 18A's (6LysAAA) showed expression levels that were approximately 35% of the HA-YFP control, while 27 and 36A's (9 and 12LysAAA) constructs were at the limit of detection (FIG. 26E). Insertion of 12LysAAG codons in the fusion protein, showed 6- to 8-fold reduction in expression of fusion protein. Since the different fusion proteins were all transcribed from the MTT1 promoter under identical induction conditions, we reasoned that amount of mRNA produced for each construct should be equivalent. We used qRT-PCR to quantify the steady state level of YFP mRNA of each fusion (FIG. 26F). The steady-state mRNA levels of polyA track-YFP constructs strongly reflected the decreasing YFP protein accumulation relative to the WT. Insertion of 18As (6LysAAA codons) reduced mRNA levels to approximately 30-35% of WT levels, while insertion of 27 and 36As (9 and 12LysAAA codons, respectively) reduced mRNA levels to less than 5% of the HA-YFP construct (FIG. 26D). Interestingly, while the attenuation at the protein level was stronger for the insertion of 12LysAAG codons than for 6LysAAA codons the trend was lost at mRNA levels. This can be due to the different pathways that resolve polybasic peptide stalling and polyA track-induced stalling and frameshifting in eukaryotic cells (Arthur, et al., 2015; Koutmou, et al., 2015). Nonetheless, we were able to control expression of reporter genes using polyA tracks in a similar manner in T. thermophila, a single cell AT-rich protozoan, as we did previously in S. cerevisiae and above mentioned E. coli cells (Koutmou, et al., 2015).

EXAMPLE 4: PolyA Tracks can be Used for Gene Expression Regulation in Plant Tissues

To test whether polyA tracks can attenuate gene expression in plants, we transiently co-expressed HA-polyA-mCherry with an YFP construct as internal control in the model plant Nicotiana benthamiana (FIG. 33 ). The expression of mCherry and YFP was assessed by fluorescence imaging (FIG. 27A). Like single cell cultures, N. benthamiana epidermal cells showed attenuated mCherry fluorescence proportional to the length of the polyA tracks (6,9 and 12 LysAAA codons) compared to the HA-mCherry and 12 LysAAG control constructs (FIG. 27A). The fluorescence data for each construct revealed the same trend of gene expression regulation as in T. thermophila cells (FIG. 26D). As fluorescence in this assay was not quantifiable, protein abundance was determined by semi-quantitative Western blot analysis of N. benthamiana leaves infiltrated with the HA-polyA-mCherry. The levels of HA-mCherry proteins were normalized to levels of the cis-linked selectable marker phosphinotricin acetyl transferase (BAR) in the same sample (FIG. 27B and FIG. 27C). The addition of a polyA track with 18As (6 LysAAA) decreased protein accumulation to approximately 70% of HA-mCherry levels. Further reduction of mCherry protein accumulation, to 30% and below detection limit was observed in 9 LysAAA and 12 LysAAA constructs, respectively (FIG. 27C). Parallel analyses of steady state mRNA levels of transcripts with increasing lengths of polyA tracks showed progressively reduced levels of polyA track mRNAs when compared to transcript levels of the HA-mCherry and AAG-containing control constructs (FIG. 27D). mRNA levels were reduced to approximately 50-55% of WT expression for 6LysAAA transcripts, while 9 and 12LysAAA constructs had reduced mRNA levels to approximately 30 and 20% of controls, respectively (FIG. 27D). These results indicate that polyA tracks affect both mRNA and protein levels and can be used to regulate the gene expression in plants.

EXAMPLE 5: PolyA Tracks can be Used to Regulate Gene Expression in Human Tissue Cultures

To further assess the universality of polyA tracks on protein expression, we tested our reporter series in human tissue cultures using HeLa cells. Plasmids with HA-mCherry, HA-12LysAAG-mCherry and HA-polyA-mCherry reporters, driven by the constitutively active CMV promoter, were electroporated into HeLa cells for transient expression. Protein abundances were assessed by Western blot analyses 24 hours after electroporation (FIG. 27E). As in our previous study on expression of endogenous and synthetic polyA tracks in various human tissue cultures (Arthur, et al., 2015), constructs with increasing length of polyA tracks (6, 9 and 12 LysAAA) were expressed less than control constructs and reduction in protein expression was proportional with the length of polyA track. Construct with 18As (6LysAAA) displayed approximately 3-fold reduction in expression compared to WT construct. Insertion of 27 and 36As (9 and 12LysAAA, respectively), exhibited 6 and 25-fold reduction of HA-mCherry expression compared to WT (FIG. 27F). Our control construct with 12LysAAG codons did not show any reduction in protein levels compared to WT construct (FIG. 27E and FIG. 27F). This again indicates differences between translational stalling induced by polybasic peptides (Arthur, et al., 2015; Koutmou, et al., 2015; Kuroha, et al., 2010; Brandman, et al., 2012), which seems to be cell or organism specific and unpredictable, and polyA track-induced ribosomal stalling and frameshifting (Arthur, et al., 2015; Koutmou, et al., 2015) which is clearly dependent on the length of polyA tracks and conserved between multiple organisms and tissue cultures. mRNA stability of the reporters corresponded to protein expression as it was seen in our previous report (data not shown) (Arthur, et al., 2015). Together with our previous study (Arthur, et al., 2015), our results indicate that polyA tracks can easily be used to regulate expression of reporters or genes transiently transfected in diverse eukaryotic tissues and cultured cell systems, such as N. benthamiana and human cell cultures, as well as other mammalian or insect tissue culture systems (Arthur, et al., 2015).

EXAMPLE 6: PolyA Tracks can be Used for Gene Expression Regulation in all Tissues of Model Organism

We next sought to test whether polyA tracks can be used to regulate reporter gene expression in complex, multicellular organisms. We chose fruit fly, D. melanogaster, due to the well-developed tools in the manipulation of endogenous genetic loci, as well as for the easier assessment of our mCherry reporter screen. Using the PhiC31-integrase approach (Groth, et al., 2004), we generated single transgene insertions of the HA-mCherry and HA-12LysAAG-mCherry controls, and HA-polyA-mCherry (6, 9 and 12LysAAA) constructs in the identical genomic location in the third chromosome (FIG. 34 ). All constructs contained Upstream Activation Sequence (UAS) followed by HSP70 promoter which actively transcribes mCherry reporter mRNAs in response to expression of GAL4 protein (Duffy, 2002). To drive expression of mCherry in all tissues, each transgenic line was crossed to a line that carried the Tub-GAL4 driver line that expresses GAL4 protein in all tissues and a UAS-linked GFP transgene, which allowed us to use GFP expression for normalization of the mCherry reporter genes (FIG. 34 ).

Expression of mCherry was assessed by fluorescence imaging of formaldehyde fixed salivary glands (SG), central nervous system (CNS), and proventriculus (PV) dissected from otherwise wild-type third instar larvae (FIG. 32A). Wild type HA-mCherry expressed well in all imaged tissues. Addition of a polyA track with 18A's (6LysAAA) reduced mCherry expression to approximately 30% of the wild type construct in all three tissues (FIG. 28B, FIG. 28C, FIG. 28D, and FIG. 35 ). Constructs with 27As and 36As (9 and 12LysAAA codons, respectively) reduced expression of mCherry in all assayed tissues to approximately 20% and 10% of wild type levels, respectively (FIG. 28B, FIG. 28C, FIG. 28D, and FIG. 35 ). Western blot analysis on cell lysates produced from five fruit fly larvae for each independent construct confirmed our quantification of fluorescence imaging data (FIG. 40 ). As in the previous experiments with T. Thermophila and tissue cultures (FIG. 30 and FIG. 31 ), mRNA stability of polyA track constructs in fruit fly larvae showed inverse correlation with the length of polyA track (FIG. 36 ) and concordance with protein abundances measured by Western blot analyses. Insertion of 12LysAAG codons had moderate effect on levels of mCherry mRNA and protein and was in the range of 18As (6LysAAA) insertion construct (FIG. 28B, FIG. 28C, FIG. 28D, FIG. 36 , and FIG. 36 ). Our data indicate that individual tissues of a complex multicellular organism, such as fruit fly, are equally sensitive to gene expression attenuation mediated by polyA tracks. Therefore, one can use polyA track constructs to create hypomorphic alleles and allelic series, in complex multicellular organisms with similar relative gene expression attenuation efficiency in the different tissues.

EXAMPLE 7: PolyA Tracks Control Gene Expression Independently of the Promoter Strength

Our data from fruit fly experiment indicated that the ratio between reporters with polyA track insertion and control is maintained in all tissues (FIG. 27B, FIG. 27C, FIG. 27D, FIG. 35 , FIG. 36 , FIG. 37 ). This suggests that inserted polyA tracks maintain their capacity of gene regulation independently of the strength of mRNA transcription, which is known to have a large dynamic range across genes and cell types (Li, et al., 2014).

To systematically evaluate how differences in the strength of transcription would affect gene regulation and hypomorphic expression of reporters with polyA track insertion, we used human Flp-InTM T-RexTM 293 cell lines. Using a protocol for generation of stable and inducible expression cell lines, we have generated cells with a single insertion of our mCherry control and 36A polyA track construct in the defined chromosomal locus (FIG. 38 ). The strength of transcription in these cell lines was varied by use of increasing amounts of doxycycline (0.001 to 0.1 mg/ml of Dox) present in the growth media and levels of transcription was assayed in relation to constitutively expressed hygromycin B phosphotransferase. Dose-dependence response of doxycycline-inducible CMV promoter for both polyA track and control mCherry transcript ranged over two orders of magnitude. At the same time, relative expression of polyA track construct was kept constant at 5-8% of expression of control construct based on the Western blot analysis (FIG. 29A and FIG. 29B). Moreover, relative mRNA levels of control and polyA track constructs measured by the normalized ratios did not change under different transcriptional strengths (FIG. 29C). The steady state amount of 36As polyA track construct was constantly in the range between 1-3% of the normalized control construct. The same results are obtained using stable cell lines that express HA-tagged human hemoglobin (delta chain, WT-HBD) and an 18As HBD construct (HBD-6LysAAA) with polyA track inserted in the second exon of the HBD coding sequence (FIG. 39 ). Expression of the HBD-6LysAAA protein was 3-fold reduced compared to WT-HBD construct, based on Western blot analysis (FIG. 40 ), and mRNA levels were approximately 20% of the HBD-WT mRNA levels, measured by qRT-PCR (FIG. 41 ). The relative ratios of WT-HBD and HBD-6LysAAA protein and mRNA levels were constant for different doxycycline induction levels. Together with previous data, showing regulated expression of mCherry reporter in different tissues of the transgenic fruit fly, these data demonstrate that polyA tracks can control gene expression independently of the promoter strength associated with assayed gene, keeping relative ratio of the protein levels between wild type and polyA track-attenuated product constant.

EXAMPLE 8: PolyA-Tracks can be Used to Create Sets of Hypomorphic Mutants in Functional Genes

The polyA tracks are mainly composed of lysine residues, AAA or AAG codons, which can be problematic when expressed as tags due to their charge and specific modifications (ubiquitination, acetylation, SUMOylition and hydroxylation). These features of poly-lys chains can further influence protein function as well as cell homeostasis (Brandman, et al., 2012; Dimitrova, et al., 2009; Choe, et al., 2016; Yonashiro, et al., 2016).

We tested our ability to regulate gene expression of functional proteins in both prokaryotic and eukaryotic cell system. In E. coli, the chloramphenicol acetyltransferase (CAT) gene confers resistance to the broad spectrum antibiotic chloramphenicol (CAM) in a dose-dependent manner (Shaw, et al., 1991). To show that we can regulate expression of CAT protein by insertion of polyA tracks we assessed E. coli survival under increasing concentrations of CAM in comparison with wild type CAT gene. To control for the influence of additional lysine residues in the N-terminus of CAT protein we also inserted 10LysAAG codons in the N-terminus of CAT gene. Expression of WT-CAT, AAG10-CAT and polyA-CAT constructs was driven by the inducible arabinose promoter (pBAD, FIG. 42 ). All E. coli cultures were pulse induced, with addition of 0.1% arabinose, and growth was monitored on LB plates using different amounts of CAM in the media. WT-CAT and AAG10-CAT control constructs were able to survive CAM selection to the same level of CAM concentration in the media (75 mg/ml CAM, FIG. 30A). Therefore, the function of CAT protein is not affected by the addition of 10 consecutive Lys residues. PolyA tracks in constructs led to increased CAM sensitivity, of E. coli cells, which correlated with the length of the polyA tracks inserted in CAT gene (FIG. 30A). While majority of constructs could grow on minimal addition of CAM in the media (15 mg/ml), constructs with 24, 27 or 30As (8, 9 and 10LysAAA) were unable to grow on LB-plates with CAM concentration of 30 mg/ml. Furthermore, survivability of E. coli cells with CAT constructs having 15, 18 and 21As (5, 6 and 7LysAAA) on one hand, and 9 and 12As (3 and 4LysAAA) on the other hand, was impaired when cells were grown on LB-plates with final CAM concentrations of 50 mg/ml or 75 mg/ml, respectively (FIG. 30A). The survivability of E. coli cultures with different CAT constructs was in concordance with expression levels of CAT protein assayed by Western blot analyses (FIG. 43 ). The insertion of 10LysAAG codons in CAT gene did not affect E. coli cell growth on CAM selective media or levels of CAT protein expression arguing that insertion of multiple lysine residues in the N-terminus is not detrimental for the function and stability of CAT protein. These data demonstrate that polyA tracks can regulate levels of certain enzyme expression (CAT) in E. coli cells proportionally with their length.

To test ability of polyA tracks to regulate expression and function of protein in a eukaryotic cell we monitored how polyA tracts affect expression of N-succinyl-5-aminoimidazole-4-carboxamide ribotide synthetase (Ade1) in Saccharomyces cerevisiae (FIG. 30B). Disruption of the ADE1 gene results in the storage of a red pigment due to the buildup of a metabolic byproduct of the adenine biosynthesis pathway. Yeast cells that are ade1Δ are a dark red color; reintroduction of functional Ade1 protein restores the wild type white coloration in a dose-dependent manner. Differences in colony color and ability to grown on adenine dropout media (SD-Ade) have been utilized to differentiate strains of yeast prions (Liebman, et al., 2012), assess mitotic stability (Hieter, et al., 1985), and monitor gene expression (Mano, et al., 2013).

To survey how polyA tracts affect expression of Ade1, we transformed ade1Δ strains of S. cerevisiae with single copy plasm ids (p416) encoding polyA-ADE1-FLAG, with the polyA tracks containing 18, 27 or 36As (6, 9, or 12 LysAAA, FIG. 44 ). Control plasmids contained no insertions (WT) or 12 LysAAG codons. Transformants were spotted onto plates to monitor color phenotype and growth on media lacking adenine (SD-Ade, FIG. 30B). The empty vector control exhibited a dark red coloration and inability to grow on SD-Ade, consistent with disruption of the ADE1 locus, while the wild type Ade1-FLAG restored both the white phenotype and growth on SD-Ade. Yeasts containing constructs with polyA track length of 18, 27 and 36A showed progressively pinker coloration and poorer growth on SD-Ade; however, the control 12LysAAG construct conferred a nearly-WT white color and strong growth on SD-Ade (FIG. 30B). Dot blot analysis of Ade1 protein expression, normalized to total protein, was in accordance with our phenotypic results and revealed visibly reduced amounts of expression for constructs with insertion of 9 and 12LysAAA codons (FIG. 44 ). Expression of Ade1 protein with 12 lysine residues at the N-terminus, as in the case of 12LysAAG, did not impair function of the assayed protein (Ade1) and show similar results as insertion of 6LysAAA codons. Therefore, addition of polyA tracks to functional genes in both E. coli and S. cerevisiae preserved protein function but regulated protein abundance and as such polyA tracks could potentially be used in creation of hypomorphic gene mutants with fixed levels of protein expression.

METHODS FOR EXAMPLES 2-8 E. COLI EXPERIMENTS

mCherry reporter constructs used for expression in E. coli cells were subcloned using LR clonase recombination (Thermo Fisher Scientific) from pENTR/D-Topo constructs used in this study or in previous studies (Arthur, et al., 2015; Koutmou, et al., 2015). The resulting pBAD-DEST49 vector constructs express Thioredoxin (Thrdx) fusion protein as Thrdx-HA tag-insert-mCherry. For assaying expression of mCherry reporter all constructs were expressed in 2 ml E. coli Top10 strain grown in LB-Carbencilin (LB-Carb; final concentration 100 ug/ml). The cells were grown to optical optical density at 600 nm (0D600) of 0.4 at 37° C. and induced with addition of arabinose (0.5% w/v). Fluorescence of mCherry reporter for each construct was measured in triplicates 2 to 4 hours after induction using Biotek Synergy H4 plate reader (Excitation 475±9, Emission 620±9). The amount of fluorescence was normalized to number of cells measured by OD600. To additionally check for expression of fusion proteins, 200 ul of the cells was harvested 2 hr post-induction, resuspended in 100 ul of 2xSDS sample buffer and analyzed by SDS-PAGE followed by western blot analysis using HA-tag specific probe. Images of western blot analyses were generated by Bio-Rad Molecular Imager ChemiDoc XRS System with Image Lab software for chemiluminescence detection.

The chloramphenicol acetyltransferase (CAT) constructs used for functional protein studies were created by amplification of the CAT gene from pENTR/D-Topo vector (Thermo Fisher Scientific) using primers listed in Table 6. Constructs were subcloned into pBAD-DEST49 vector for use in functional assays. E. coli Top10 cells freshly transformed with pBAD-DEST49 plasmids expressing CAT reporters with different polyA tracks as well as CAT control reporters were grown in liquid LB-Carb media (100 ug/ml). For the chloramphenicol (CAM) survivability assay E. coli cells were grown to OD600=0.4 and non-induced (NI) fractions were spotted on LB-Carb plates (Carb 100 ug/ml) without chloramphenicol or to LB-Carb/CAM plates with raising amount of chloramphenicol in the media (CAM 15-100 ug/ml). The residual amount of the cells was induced for 1 hour with arabinose (final concentration 0.1% (w/v)). Cells were washed twice in M9 minimal media, resuspended in the staring volume of LB-Carb media and 5 ul of cells was spotted as induced (I) fraction on LB-Carb and LB-Carb-CAM plates. Plates were incubated overnight at 37° C. and imaged 24 hours post induction using Bio-Rad Molecular Imager ChemiDoc XRS System.

TABLE 6 Oligos used for generation of E. coli expressing CAT constructs SEQ Construct/ ID Oligo NO: Name Primer Sequence 27 CAT WT For CACCATGCACCATCACCATCACCATGAAA AAAAAATCACTGGATATACCACCGTTGATA TATCCC 28 CAT 10xAAG CACCATGCACCATCACCATCACCATGAG AAGAAGAAGAAGAAGAAGAAGAAGAAGA AGATCACTGGATATACCACCGTTGATATA TCCC 29 CAT 3xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAATCACTGGATATACCACCGTT GATATATCCC 30 CAT 4xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAATCACTGGATATACCACC GTTGATATATCCC 31 CAT 5xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAAAAATCACTGGATATACC ACCGTTGATATATCCC 32 CAT 6xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAAAAATCACTGGATAT ACCACCGTTGATATATCCC 33 CAT 7xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAAAAAAAAAAATCACTGGA TATACCACCGTTGATATATCCC 34 CAT 8xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAAAAAAAAAAAAAATCACT GGATATACCACCGTTGATATATCCC 35 CAT 9xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAAAAAAAAAAAAAAAAATCA CTGGATATACCACCGTTGATATATCCC 36 CAT 10xAAA CACCATGCACCATCACCATCACCATGAAA AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCACTGGATATACCACCGTTGATATATCC C 37 CAT Rev CATTACAGATCTTCTTCAGAAATAAGTTTT TGTTCCGCCCCGCCCTGCCACTCATCGC AG

SACCHAROMYCES CEREVISIAE EXPERIMENTS

In order to conduct functional studies with polyA track hypomorphic attenuation in S. cerevisiae cells the ADE1 locus was deleted from 74D-964 yeast strein via homologous recombination. Resultant ade1Δ strains were transformed with an empty vector or a plasmid-based ADE1 containing variable length of polyA tracks as well as WT and 12AAG insertion constructs. Constructs were generated by performing PCR on ADE1 isolated from the yeast genomic tiling library (Open Biosystems) with primers listed in Table 6. PCR products were digested and ligated into a p416 vector backbone containing the ADE1 endogenous promotor. Clones were verified via sequencing and correct constructs were transformed into ade1Δ deletions strains via the PEG-LiOAc method (Table 6). To generate dilution spottings, three colonies were picked from each transformation plate and grown overnight in selective media. In the morning, cultures were normalized to OD600=1.0 and 10 ul of cells spotted onto rich media, SD-Ura, and SD-Ade for phenotypic analysis.

Relative protein abundance was determined via Western dot blotting. Briefly, yeast transformants were picked from selection plates to inoculate 10 mL of SD-Ura and grown overnight to ˜OD=0.6. In the morning, cells were harvested and lysed in buffer (25 mM Tris-HCl pH 7.5, 50 mM KCl, 1 mM EDTA, Roche protease inhibitor cocktail) via mechanical disruption with acid-washed glass beads (Sigma). Total protein was normalized to 1 mg/ml via Bradford assay, and 20 μg of total protein was spotted onto a nitrocellulose membrane. Western blotting was performed by overnight incubation with anti-Flag (Sigma M2, 1:1000 in 5% milk) and goat anti-rabbit (Sigma, 1:10,000 in 5% milk) antibodies followed by detection with chemiluminescence (Amersham ECL).

TABLE 7 Primers used for generation of ADE1 constructs SEQ ID No: Name Sequence 38 FwdAde1 5′GGactagtATGTCAATTACGAAGACTGAA SpelWT CTGG 39 FwdAde1  5′GGactagtATGAAAAAAAAAAAAAAAAAA Spel6AAA TCAATTACGAAGACTGAACTGG 40 FwdAde  5′GGactagtATGAAAAAAAAAAAAAAAAAA 1Spel9AAA AAAAAAAAATCAATTACGAAGACTGAACT GG 41 FwdAde1 5′GGactagtATGAAAAAAAAAAAAAAAAAA Spel12AAA AAAAAAAAAAAAAAAAAATCAATTACGAA GACTGAACTGG 42 FwdAde1 5′GGactagtATGAAGAAGAAGAAGAAGAA Spel12AAG GAAGAAGAAGAAGAAGAAGTCAATTACG AAGACTGAACTGG 43 RevAde1 5′GGatcgatTTACTTGTCGTCATCGTCCTT ClalFLAG GTAGTCGTGAGACCATTTAGACCC 44 FwdAdel 5′GGgagctcACACGATAGCAAAGCAG PromSacl 45 RevAdel 5′ GGtctagaTATCGTTAATATTTCG PromXbal

TABLE 8 S. Cerevisiae strains used in this study Name Strain Background Genotype HT 971 74D-694 Mat A, ade1::KANMX4, trp1-289(UAG), his3Δ-200, ura3-52, leu2-3, 112 HT 972 74D-694 Mat A, ade1::KANMX4, trp1-289(UAG), his3Δ-200, ura3-52, leu2-3, 112 TETRAHYMENA thermophila EXPERIMENTS

T. thermophila strain B2086 (II) was used for all experiments reported. Similar results were obtained with strain CU428 [(VII) mpr1-1/mpr1-1]. To assess the effect of polyA-tracks on protein accumulation, we modified a fluorescent protein tagging vector, pBSICY-gtw (Mott, et al., 2011) so as to fuse YFP to the carboxyl-terminus of a macronucleus-localized protein of unknown function (MLP, TTHERM_00384860), separated by a Gateway recombination cassette (Invitrogen/Life Technologies, Inc), and expressed from the cadmium inducible MTT1 promoter (Shang, et al., 2002). The MLP gene coding region was amplified with oligonucleotides 5′ ALM Bsi′ 5′-CAC CCG TAC GAA TAA AAT GAG CAT TAA TAA AGA AGA AGT-3′ (SEQ ID. No: 46) and 3′ ALM RV 5′-GAT ATC TTC AAT TTT AAT TTT TCT TCG AAG TTG C 3′ (SEQ ID NO: 47) and cloned into pENTR-D in a topoisomerase mediated reaction prior to digesting with BsiWI and EcoRV and inserting into BsiWI/PmeI digested pBSICY-gtw. Subsequently, LR Clonase II was used to insert a linker containing the sequence coding for an HA epitope tag alone (WT) or the tag plus different length of polyA tracks or AAG insertions in place of the Gateway cassette.

The expression cassette is located within the 5′ flanking region of a cycloheximide resistant allele of the rpL29 gene to direct its integration into this genomic locus. These constructs were linearized with Pvul and Sacl in the region flanking the Tetrahymena rpl29 sequences and introduced into starved Tetrahymena cells by biolistic transformation (Cassidy-Hanley, et al., 1997; Bruns, et al., 2000). Transformants were selected in 1× SPP medium containing 12.5 μg/ml cycloheximide. To control for copy number, PCR assays with primers MTT2386 5′-TCTTAGCTACGTGATTCACG-3′ (SEQ ID NO: 48) and Chx-117, 5′-ATGTGTTATTAATCGATTGAT-3′ (SEQ ID NO: 49) and Chx85r, 5′-TCTCTTTCATGCATGCTAGC-3′ (SEQ ID NO: 50) verified that all rpL29 loci contained the integrated expression construct.

Transgene expression was induced by addition of 0.4 μg/ml CdCl2 and cells were grown 12-16 hours before monitoring protein accumulation. YFP accumulation was visualized by epifluorescence microscopy as previously described (Matsuda, et al., 2010). Whole cells extracts were generated by boiling concentrated cell pellets in 1× Laemmli sample buffer, followed by were fractionation on 10% SDS polyacrylamide gels and transfer to nitrocellulose. YFP accumulation was a monitored with mouse anti-GFP antisera (G28R anti-GFP (OAEA00007) antibody, Aviva Systems Biology) and normalized to acetylated alpha Tubulin (6-11B-1 monoclonal Anti-Acetylated Tubulin antibody (T7451) Sigma-Aldrich). qPCR analysis was done using 5′-AGGCCTACAAGACCAAGGGT-3′ (SEQ ID NO: 51) and 5′-AGAGCGGTTTTGACGTTGGA-3′ (SEQ ID NO: 52) primers for T. Thermophila ribosomal protein L21 (rpl21) which was used for normalization. Primers 5′-CCCGTATGACGTACCGGATTATG-3′ (SEQ ID NO: 53) and 5′-ACTTCAGGGTCAGCTTGCC-3′ (SEQ ID NO: 54) were used for detection and estimation of fusion protein transcript levels using SybrGreen master mix and CFX96 Touch™ Real time PCR Detection System (BioRad). Normalized ΔCt values were used to calculate fold ratio between WT, 12LysAAG and polyA track constructs.

NICOTIANO BENTHAMIANA EXPERIMENTS

Constructs for expression of HA-tagged mCherry reporters that were already cloned in pEntryD-TOPO vector were sub-cloned to pEarleyGate 100 (ABRC stock number CD3-724) through LR reaction using LR clonase (Invitrogen™) The mCherry reporter constructs, pEARLY100 and pBIN61 plasmids were individually electroporated into Agrobacterium tumefaciens strains GV3101 (Koncz, et al., 1986). The strain carrying pBIN61 construct expressing p19 protein from tomato bushy stunt virus was co-infiltrated with the reporter constructs to suppress post-transcriptional gene silencing (Voinnet, et al., 2003). The Agrobacterium suspensions carrying the reporter constructs were infiltrated into the leaves of 5- to 6-week-old N. benthamiana plants as described in Joensuu, J. J. et al. Briefly, saturated over-night cultures were spun-down and resuspended in the infiltration solution (3.2 g/L Gamborg's B5 plus vitamins, 20 g/L sucrose, 10 mM MES pH 5.6, 200 μM 4′-Hydroxy-3′,5′-dimethoxyacetophenone) to a final OD600=1.0; Agrobacterium suspensions carrying the reporter constructs were individually mixed with suspensions carrying the pBIN61 construct in 1:1 ratio prior to infiltrations. These suspensions were infiltrated into separate segments of two young leaves on each of eight different N. benthamiana plants, which served as biological replicates. For control, 1:1 suspension of A. tumefaciens carrying pEARLY 100 with no insert along with pBIN61 was used. The infiltrated plants were maintained in a controlled growth chamber conditions at 22° C., with a 16h photoperiod.

Samples of the abaxial epidermis of N. benthamiana leaves infiltrated with different mCherry reporter constructs were collected 6 days post-infiltration. Infiltration was performed as described in the previous section, with the addition of an YFP-expressing construct pEARLY104 (ABRC stock number CD3-686), which served as infiltration control. The samples were visualized for fluorescence by confocal laser-scanning microscopy using a Leica TCS SP2 confocal microscope.Samples for RNA and total soluble protein (TSP) extraction were separately collected from the infiltrated plants 6 days post-infiltration using a cork borer (7.1 mm in diameter); each sample contained equal amounts of leaf tissue (2 leaf discs) collected from each of the segments on the two leaves infiltrated with the same construct.

Analysis of mCherry protein accumulation was carried out by Western blot as described in Gutiérrez et al., 2013 and Conley et al., 2009. Briefly, phosphate-buffered saline (PBS: 8 g/L NaCl, 1.16 g/L Na2HPO4, 0.2 g/L KH2PO4, 0.2 g/L KCl, pH 7.4), supplemented with 1 mM EDTA, 1 mM phenylmethanesulfonylfluoride (PMSF), 1 μg/ml leupeptin 0.1% Tween-20 and 100 mM sodium L-ascorbate was used for total soluble protein (TSP) extractions. Bradford assay (Biorad) was used to quantify TSP in the extracts using a standard curve (r2=0.99) of known concentrations of Bovine Serum Albumin (BSA). Sample extracts (25 μg TSP for mCherry and 5 μg TSP for phosphinotricin acetyl transferase [BAR] protein detection) were separated by SDS-PAGE, blotted onto nitrocellulose membrane and probed with a primary anti-HA tag antibody (Genscript) for mCherry, or anti-Phosphinotricin acetyl transferase antibody (Abcam) for BAR, both at 1:2000 dilution, followed by HRP-conjugated secondary antibody (Biorad) at 1:5000 dilution. The blots were washed (3 times×10 min) in 1×Tris-buffered Saline (TBS, 50 mM Tris, 150 mM NaCl, pH 7.5) containing 0.1% Tween (Sigma) and images were obtained after 1 min incubation with the enhanced chemiluminescence (ECL) detection system (GE Healthcare). Numerical values for protein accumulation were derived from the detected band intensities on the analyzed images using TotalLab TL 100 software (Nonlinear Dynamics, Durham, USA). The mCherry accumulation values were normalized for Basta accumulation detected in the same sample. Normalized values of the mCherry protein accumulation for each reporter construct were presented as the mean of eight biological replicates±SE; Tukey's honest significance test (JMP software, SAS Institute Inc.) was used to identify significantly different means (α=0.05).

For quantitative RT-PCR (qPCR), total RNA was extracted using an RNeasy plant mini kit coupled with DNase treatment (Qiagen). The purified RNA (500 ng) was reverse-transcribed using the Maxima first-strand cDNA synthesis kit (Thermo Fisher Scientific). The resulting cDNA (2 ng/μl) was quantified by qPCR using the Maxima SYBR Green/ROX qPCR master mix (Thermo Fisher Scientific) and CFX384 Touch™ Real-Time PCR Detection System (Biorad). Cycle threshold (Ct) values were normalized to phosphinothricin N-acetyltransferase (BAR) gene expressed in the same plasmid used for transient expression. Primer sequences used: For mCherry-mCherryFWD: 5′-GGCTACCCATACGATGTTCC-3′(SEQ ID NO: 55); mCherryREV: 5′-CCTCCATGTGCACCTTGAAG-3′ (SEQ ID NO: 56); for BASTA-BAR-F3: 5′-TCAAGAGCGTGGTCGCTG-3′ (SEQ ID NO: 57) and BAR-R3: 5′-CAAATCTCGGTGACGGGCAG-3′ (SEQ ID NO: 58).

DROSOPHILA MELANOGASTER EXPERIMENTS

Reporter gene expression was achieved with the GAL4/UAS system. The UAS-mCherry transgene plasmids were constructed from the phiC31 integrase plasmid, pJFRC28-10XUAS-IVS-GFP-p10 (Addgene plasmid #36431) (Pfeiffer, et al., 2012). GFP was removed by digestion with Kpnl and Xbal and replaced with HA-mCherry and HA-polyA-mCherry. Transgenic fly lines were obtained by injecting P{CaryP}attP2 embryos with each pJFRC28 mCherry construct to achieve site-specific, single insertion on the third chromosome at the attP2 landing site (Rainbow Transgenic Flies, Inc.). Injected GO adult flies were backcrossed to w1118 flies. Red-eyed progeny indicated successful germline integration of the UAS-mCherry expression cassette. Male red-eye progeny were crossed to female w;TM3 Sb/TM6 Tb flies followed by sib-crosses of the F1 progeny to generate homozygous UAS-mCherry transgenic lines. Insertion was confirmed by Sanger sequencing of PCR amplified mCherry from genomic DNA of individual flies. Each mCherry transgenic fly line was crossed to a TubGal4 UAS-GFP driver line (derived from BSC42734) to achieve mCherry expression in all tissues. GFP expression was used for normalization. All flies were maintained at 25° C.

Third instar larvae from each cross were fixed in formaldehyde and dissected to recover the salivary glands (SG), intact central nervous system (CNS), and proventriculus (PV). The tissues were mounted on glass cover slips and confocal images were taken on a Zeiss Imager 2 upright microscope using identical parameters for all images of each tissue type. Fluorescence intensity of the mCherry and GFP were quantified with Zen 9 software.

Total RNA was extracted from each cross by pooling 5 third instar larvae in 1.5 ml RNase-free Eppendorf tubes which were then frozen in dry ice. Frozen samples were homogenized using 1.5 ml pestles (Fisherbrand, RNase- and DNase-free). After homogenization, 1 ml RiboZol reagent (Amresco) was added and extraction was completed according to manufacturer's instructions. Total RNA samples were treated with TURBO DNA-free kit (Ambion) to remove potential genomic DNA. cDNA synthesis was performed with iScript Reverse Transcription Supermix (Bio-Rad) with 1 μg of total RNA in a 20 μl reaction. RT-qPCR was performed in the Bio-Rad CFX96 Real-Time System with iQ SYBR Green Supermix (Bio-Rad). The mCherry transcript was detected with the following primers: 5′-TGACGTACCGGATTATGCAA-3′ (SEQ ID NO: 59) and 5′-ATATGAACTGAGGGGACAGG-3′ (SEQ ID NO: 60). Cycle threshold (Ct) values were normalized to EF1 with the following primers: 5′-GCGTGGGTTTGTGATCAGTT-3′ (SEQ ID NO: 61) and 5′-GATCTTCTCCTTGCCCATCC-3′ (SEQ ID NO: 62)) (Ponton, et al., 2011).

For western blot analysis, five third instar larvae from each cross were collected and frozen in dry ice. Frozen samples were homogenized using 1.5 ml pestles (Fisherbrand, RNase- and DNase-free). After homogenization, SDS sample buffer was added and the samples were boiled for 10 minutes. Anti-HA was used to detect mCherry expression. Samples were normalized with anti-GFP.

H. sapiens Cell Culture Experiments

mCherry reporter constructs used for transient expression in human cells were subcloned using LR clonase recombination (Thermo Fisher Scientific) from pEntryD-Topo constructs used in other experiments or in previous studies (Arthur, et al., 2015). DNA fragments for constructs used for creation of inducible and stable cell lines were PCR amplified, purified and ligated into pcDNA 5/FRT/TO vector (Thermo Fisher Scientific).

HeLa cells were cultured in Dulbecco's modified Eagle's medium (DMEM) (Gibco) and supplemented with 10% fetal bovine serum, 5% minimum essential medium nonessential amino acids (100×, Gibco), 5% penicillin and streptomycin (Gibco), and L-glutamine (Gibco). Flp-In T-REx Hek-293 cells were grown in the same media with addition of 5 ug/ml of blastocidin and 100 ug/ml of Zeocin for non-recombined cells, or 5 ug/ml of blastocidin and 100 ug/ml of hygromycin for growth of stable cell lines expressing mCherry or HBD constructs.

Plasmids were introduced to the tissue culture cells by the Neon Transfection System (Thermo Fisher Scientific) using 100-μl tips according to cell-specific protocols (www.lifetechnologies.com/us/en/home/life-science/cell-culture/transfection/transfection-selection-misc/neon-transfection-system/neon-protocols-cell-line-data.html). Hela cells, used for transient expression, were electroporated with 1.5 ug of DNA plasmids and were harvested 24 hours after the electroporation. Flp-In T-REx Hek-293 cells were electroporated with plasmids, selected for positive clones as described by protocol (https://tools.thermofishercom/content/sfs/manuals/flpinsystem_man.pdf). Expression of polyA track and control constructs was induced by addition of various amounts of doxycycline from a common stock (1 μg/ml) and harvested 24 or 48 hours after induction, if not indicated differently.

Total RNA was extracted from cells using the RiboZol RNA extraction reagent (Amresco) according to the manufacturer's instructions or using GenElute™ Direct. RiboZol reagent (500 μl) was used in each well of 6- or 12-well plates for RNA extraction. Precipitated nucleic acids were treated with Turbo deoxyribonuclease (Ambion), and total RNA was dissolved in ribonuclease-free water and stored at −20° C. RNA concentration was measured by NanoDrop (0D260/280). iScript Reverse Transcription Supermix (Bio-Rad) was used with 1 μg of total RNA following the manufacturer's protocol. RT-qPCR was performed in the Bio-Rad CFX96 Real-Time System with iQ SYBR Green Supermix (Bio-Rad). For both transient expression samples and stable cell line samples, the mCherry transcript was detected with the following primers: 5′-TGACGTACCGGATTATGCAA-3′ (SEQ ID NO: 63) and 5′-ATATGAACTGAGGGGACAGG-3′ (SEQ ID NO: 64). Cycle threshold (Ct) values were normalized to the neomycin resistance gene expressed from the same plasmid for transient expression (5′-CTGAATGAACTGCAGGACGA-3′ (SEQ ID NO: 65) and 5′-ATACTTTCTCGGCAGGAGCA-3′ (SEQ ID NO: 66)) or hygromycin (5′-GATGTAGGAGGGCGTGGATA-3′ (SEQ ID NO: 67) and 5′-ATAGGTCAGGCTCTCGCTGA-3′ (SEQ ID NO: 68) or actin gene for stable cell lines (5′-AGAAAATCTGGCACCACACC-3′ (SEQ ID NO: 69) and 5′-AGAGGCGTACAGGGATAGCA-3′ (SEQ ID NO: 70).

Total cell lysates were prepared with passive lysis buffer (Promega). Blots were blocked with 5% milk in 1× tris-buffered saline-0.1% Tween 20 (TBST) for 1 hour. Horseradish peroxidase-conjugated or primary antibodies were diluted according to the manufacturer's recommendations and incubated overnight with membranes. The membranes were washed four times for 5 min in TBST and prepared for imaging, or secondary antibody was added for additional 1 hour of incubation. Images were generated by Bio-Rad Molecular Imager ChemiDoc XRS System with Image Lab software by chemiluminescence detection or by the LI-COR Odyssey Infrared Imaging System. Blots imaged by the LI-COR system were first incubated for 1 hour with Pierce DyLight secondary antibodies.

Discussion for EXAMPLES 2-8

We have presented a rapid method of generating hypomorphic mutations in a reporter or gene of interest. Insertion of a polyA track into a coding sequence shows predictable and robust attenuation of gene expression in all tested cell culture and model organism systems. The length of the polyA track can be manipulated to achieve full-range of expression levels, allowing for the generation of an allelic series from complete knockout to wild-type expression for the study of gene function. This method can also be used in synthetic biology applications that require precise gene control and modeling of metabolic and signaling networks (Chuang, et al., 2010).

The use of polyA tracks overcomes many of the challenges present in current methods of generating hypomorphic mutations and controllable gene expression. For instance, a recent approach to attenuate gene expression in E. coli is mutagenesis of the Shine-Dalgarno sequence in the gene of interest. The expression levels from all possible six-mer Shine-Dalgarno sequences were experimentally determined and the information is available in the EMOPEC database (Bonde, et al., 2016). However, this valuable resource would have to be generated anew to use this approach in other prokaryotes and it could not be used in eukaryotic systems. Additionally, many orthogonal translation systems rely on modified Shine-Dalgarno sequences (Hui, et al., 1987; Hui, et al., Methods Enzymol., 1987; Lee, et al., 1996; Rackham, et al., 2005). Use of an orthogonal translation system would prohibit use of the Shine-Dalgarno sequence for expression regulation. The polyA track system of gene regulation and creation of hypomorphic mutations overcomes this issue due to its dependency on regulation of translation elongation cycle which is conserved between prokaryotes and eukaryotes (Melnikov, et al., 2012).

Hypomorphic mutations have been generated in eukaryotic cell systems by insertion of an antibiotic resistance gene into introns (Meyers, et al., 1998) or the 3′-untranslated region of genes (Breslow, et al., 2008). Insertion of the neomycin resistance gene (neo) into an intron introduces a cryptic splice site that causes aberrant splicing of transcripts, effectively reducing gene expression (Meyers, et al., 1998). The reliance on stochastic cryptic splicing events leads to unpredictable changes in transcript expression and is rather gene dependent. Insertion of neo in various genes have resulted in expression of a functionally null allele (Nagy, et al., 1998), hypomorphic expression(Meyers, et al., 1998; Hirotsune, et al., 1998), or no change in expression (Wolpowitz, et al., 2000). Our system of polyA tracks gives predictable gene expression attenuation in variety of different eukaryotic systems and, furthermore, shows relative gene expression attenuation efficiency in the different tissues of the same organism.

We have primarily introduced polyA tracks at the N-terminal regions of reporter genes due to the uniformity of the construct design and to reduce potential frameshifting effects (Arthur, et al., 2015; Koutmou, et al., 2015). We do not anticipate this to be a major limitation of this method. Our Tetrahymena reporters place the polyA tracts at the N-terminus of YFP, but at the C-terminus of the linked Tetrahymena gene (FIG. 32 ). Furthermore, insertion of polyA track in the second exon of the human beta globin gene (HBD) gene, an unstructured loop of the protein, argue that polyA tracks can be introduced at various positions in the gene (FIG. 39 , FIG. 40 , and FIG. 41 ). Additionally, we have shown previously that naturally occurring polyA track sequences exist in the human genome and that potential frameshifted products are efficiently degraded by non-sense mediated decay mechanisms (Arthur, et al., 2015).

PolyA tracks that are used endogenously in eukaryotic genomes are typically interrupted by other nucleotides at various positions within the A-rich sequence. We have observed that the position of the interrupting nucleotide, in combination with the length of the A-rich sequence, modulate gene expression (Arthur, et al., 2015). This characteristic indicates that polyA mediated regulation can be further developed for even more precise control of gene expression. Lastly, approximately 2% of human genes are endogenously regulated by polyA tracks, including many well-studied, disease-associated genes, such as BRCA1, TCOF1 and MTDH among others (Arthur, et al., 2015; Habich, et al., 2016). As we showed in our previous study, synonymous mutations of the internal polyA track of such genes can allow investigators to dramatically change expression levels of these genes without manipulation of protein sequence or the gene regulatory elements such as promoters and enhancers (Arthur, et al., 2015).

The addition of a polyA track to the target gene will result in additional lysine residues in the protein product. Like any protein tag, it is important to consider the effects of the additional residues when studying the functionality of the protein. We have shown that the function and stability of two structurally diverse proteins, CAT and Ade1, are not affected by up to 12 additional lysine residues. To control for possible effects of the poly-lysine tracks, investigators can create an allele with the same number of lysine residues encoded by AAG codons. The AAG codons will have minimal effect on expression levels while encoding a synonymous protein. Furthermore, the flexibility in polyA track placement within the coding sequence allows investigators to choose the most suitable insertion site for the protein of interest.

The conservation of the polyA track sequences in the multiple genes across vertebrates as well as our analysis of mutation rates of polyA tracks (36As) inserted in the defined locus of D. melanogaster genome argue that polyA tracks can be used to create stable hypomorphic gene alleles. Our results are in the range of already described hypermutability (approximately 8%) of the short tandem repeats (STRs) and BAT-40 microsatellite (40As) located in the second intron of the 3-beta-hydroxysteroid dehydrogenase gene. The distinction is that our data show general mutation rates for the whole fruitfly after more than 30 generations while in the case of the mentioned study28 the mutation rate is dependent on the cell type. An additional study found that the mutation rate in polyA region, 10As in this case, is in the range of 10-4 per cell per generation. As such, the authors argue that approximately 1% of cells will be affected by a polyA region mutation in 100 generations. Similar rates were observed in the other studies with approximately 10⁻⁶-10⁻² mutation rate for the different lengths of homopolymeric regions or STRs. PolyA tracks used in our study tend to operate on the shorter side of the length distribution of STRs and as such should have similar if not even lower rates of mutations.

PolyA tracks that are used endogenously in eukaryotic genomes are typically interrupted by other nucleotides at various positions within the A-rich sequence, which further reduces potential hypermutability effects. We have observed that the position of the interrupting nucleotide or codon, in combination with the length of the A-rich sequence, modulates gene expression (FIG. 45A-D). These observations suggest that polyA-mediated regulation can be further developed for even more precise control of gene expression. Lastly, approximately 2% of human genes are endogenously regulated by polyA tracks, including many well-studied, disease-associated genes, such as BRCA1, TCOF1 and MTDH among others. As we showed in our previous study, synonymous mutations of the internal polyA track of such genes can allow investigators to dramatically change expression levels of these genes without manipulation of protein sequence or gene regulatory elements such as promoters and enhancers. The use of our method is not restricted only to these genes, and we feel that the synthetic biology field will benefit from this application. Control of biosynthetic pathways for production of useful secondary metabolites, antibiotics, or recombinant antibodies, as well as introduction of controllable retrosynthetic and fully engineered pathways or ultimate control of metabolic pathways in the modeling of diseases are just a few among the multiple possible applications of this method in the future.

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What is claimed is:
 1. A method for modulating the level of expression of a polypeptide in a cell, the method comprising modulating the amount of consecutive adenine (A) nucleotides in at least one lysine codon in an open reading frame of a polynucleotide sequence encoding the polypeptide in the cell, thereby modulating the level of expression of the polypeptide in the cell.
 2. The method of claim 1, wherein modulating the amount of consecutive adenine nucleotides in the at least one lysine codon comprises increasing the amount of consecutive A nucleotides in the at least one lysine codon, comprising introducing at least one synonymous G to A nucleotide mutation into the at least one lysine codon in the open reading frame of the polynucleotide sequence encoding the polypeptide in the cell, thereby decreasing the level of expression of the polypeptide in the cell.
 3. The method of claim 1, wherein modulating the amount of consecutive adenine nucleotides in the at least one lysine codon comprises increasing the amount of consecutive A nucleotides in the at least one lysine codon comprising inserting at least one AAA lysine codon into the open reading frame of the polynucleotide sequence encoding the polypeptide in the cell.
 4. The method of claim 3, wherein the at least one AAA lysine codon is inserted into an open reading frame at a position selected from the group consisting of in a 5′ untranslated region (UTR), in an exon, at an exon/intron boundary, and in a 3′ UTR.
 5. The method of claim 1, wherein modulating the amount of consecutive A nucleotides in the at least one lysine codon comprises decreasing the amount of consecutive A nucleotides in the at least one lysine codon, comprising introducing at least one synonymous A to G nucleotide mutation into the at least one lysine codon in the open reading frame of the polynucleotide sequence encoding the polypeptide in the cell, thereby increasing the level of expression of the polypeptide in the cell.
 6. The method of claim 1, wherein modulating the amount of consecutive A nucleotides in the at least one lysine codon comprises decreasing the amount of consecutive A nucleotides in the at least one lysine codon comprising inserting at least one AAG lysine codon into the open reading frame of the polynucleotide sequence encoding the polypeptide in the cell.
 7. The method of claim 5, wherein the at least one AAG lysine codon is inserted into polynucleotide sequence for expression at the N-terminus or C-terminus of the polypeptide in the cell.
 8. The method of claim 1, wherein polynucleotide sequence comprises an endogenous polynucleotide sequence and the step of modulating the amount of consecutive A nucleotides in the at least one lysine codon comprises: i) selecting an endogenouous polynucleotide sequence in the cell that comprises at least one lysine codon; and ii) editing the endogenous polynucleotide sequence in the cell, wherein editing the endogenous polynucleotide sequence in the cell comprises contacting the cell with an engineered nuclease selected from the group consisting of a CRISPR-Cas system, a CRISPR-Cpf1 system, a zinc finger nuclease (ZFN), a transcription activator-like effector nuclease (TALEN), and a meganuclease, and combinations thereof.
 9. The method of claim 1, wherein the at least one lysine codon comprises at least one polylysine track selected from the group consisting of AAA lysine codons, AAG lysine codons, and combinations thereof.
 10. An expression vector comprising: a) a cloning site for inserting at least one polynucleotide sequence encoding a polypeptide to be expressed, and at least one polynucleotide tag sequence comprising at least one AAG lysine codon that increases expression of the at least one polynucleotide sequence when the expression vector is introduced into a cell; or b) a cloning site for inserting at least one polynucleotide sequence encoding a polypeptide to be expressed, and at least one polynucleotide tag sequence comprising at least one AAA lysine codon that decreases expression of the at least one polynucleotide sequence when the expression vector is introduced into a cell.
 11. The expression vector of claim 10, wherein the at least one polynucleotide tag sequence in a) comprises at least one polylysine track comprising at least two consecutive AAG lysine codons, and wherein the at least one polynucleotide tag sequence in b) comprises at least one polylysine track comprising at least two consecutive AAA lysine codons.
 12. The expression vector of claim 10, wherein the at least one polylysine track in a) comprises at least two consecutive AAG lysine codons selected from the group consisting of (AAG)2, (AAG)3, (AAG)6, and (AAG)12, and wherein the at least one polylysine track in b) comprises at least two consecutive AAA lysine codons selected from the group consisting of (AAA)2, (AAA)3, (AAA)6, and (AAA)12.
 13. An expression vector comprising: a) at least one engineered polynucleotide sequence encoding a polypeptide to be expressed, the at least one engineered polynucleotide sequence comprising at least one engineered synonymous mutation of at least one AAA lysine codon to at least one AAG lysine codon in a coding sequence of the at least one polynucleotide sequence, wherein the synonymous mutation increases expression of the polypeptide to be expressed when the expression vector is introduced into a cell; or b) at least one engineered polynucleotide sequence encoding a polypeptide to be expressed, the at least one engineered polynucleotide sequence comprising at least one engineered synonymous mutation of at least one AAG lysine codon to at least one AAA lysine codon in a coding sequence of the at least one polynucleotide sequence, wherein the synonymous mutation decreases expression of the polypeptide to be expressed when the expression vector is introduced into a cell.
 14. The expression vector of claim 13, wherein the at least one engineered polynucleotide sequence comprises at least one polylysine track comprising at least two consecutive lysine codons in the coding sequence.
 15. The expression vector of claim 13, wherein the at least one polylysine track in a) comprises at least two consecutive AAG lysine codons selected from the group consisting of (AAG)2, (AAG)3, (AAG)6, and (AAG)12, and wherein the at least one polylysine track in b) comprises at least two consecutive AAA lysine codons selected from the group consisting of (AAA)2, (AAA)3, (AAA)6, and (AAA)12.
 16. The expression vector of claim 14, wherein the at least one polylysine track comprises at least 11 consecutive A nucleotides in at least three consecutive lysine codons, prior to enginnering the at least one engineered polynucleotide sequence to include the at least one engineered synonymous mutation.
 17. An isolated recombinant cell comprising the expression vector of claim
 10. 18. A kit comprising the expression vector of claim 10, and instructions for expressing a polypeptide of interest.
 19. An isolated recombinant cell comprising the expression vector of claim
 13. 20. A kit comprising the expression vector of claim 13, and instructions for expressing a polypeptide of interest. 